Oral composition of celecoxib for treatment of pain

ABSTRACT

The present invention relates to a stable oral liquid pharmaceutical composition of celecoxib or pharmaceutically acceptable salts thereof. The celecoxib present in the compositions as described herein do not show any precipitation when subjected in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes. It also relates to the process of preparing and method of using said composition of celecoxib.

RELATED APPLICATIONS

This application claims priority from U.S. Provisional Application No. 62/342,874, filed on May 27, 2016, the entire disclosure of which is incorporated herein by this reference.

BACKGROUND

Non-steroidal anti-inflammatory drugs (NSAID) are generally used for the treatment of acute pain, inflammatory pain, visceral pain, breakthrough pain, nociceptive pain, neuropathic pain, dysmenorrhea, post-surgical pain, acute postpartum pain, postoperative pain management, chronic pain in osteoarthritis, rheumatoid arthritis, and pain due to other diseases and causes.

Celecoxib is approved in U.S. under brand name CELEBREX®, as oral capsules, and is used in the treatment of osteoarthritis, rheumatoid arthritis, juvenile rheumatoid arthritis, ankylosing spondylitis, acute pain, chronic pain, primary dysmenorrhea and familial adenomatous polyposis. It is available in the strengths of 50 mg, 100 mg, 200 mg, and 400 mg.

Celecoxib was described in U.S. Pat. No. 5,466,823 assigned to Searle, which describes a class of 1, 5-diaryl pyrazoles and their salts together with processes for the preparation of such compounds.

Celecoxib is chemically designated as 4-[5-(4-methylphenyl)—3-(trifluoromethyl)-1H-pyrazol-1-yl] benzenesulfonamide and is a diaryl-substituted pyrazole. The empirical formula is C₁₇H₁₄F₃N₃O₂S, and the molecular weight is 381.38; the chemical structure is as follows:

U.S. Pat. No. 5,466,823 contains general references to formulations for the administration of 1,5-diaryl pyrazoles, including orally deliverable dosage forms such as tablets and capsules.

U.S. Pat. No. 5,760,068 describes a class of 1,5-diaryl pyrazole compounds including celecoxib that are selective inhibitors of cyclooxygenase-2 and can be administered to treat, among other conditions and disorders, pathological conditions associated with rheumatoid arthritis and osteoarthritis.

Celecoxib is a hydrophobic and highly permeable drug belonging to class II of biopharmaceutics classification system. Celecoxib is a neutral molecule that is essentially insoluble in water, which leads to high variability in absorption and hence has limited bioavailability after oral administration. It also has pre-systemic metabolism.

Celecoxib has an aqueous solubility of about 5 μg/ml at between 5° C. and 40° C., which is pH independent at pH<9. Celecoxib is not readily dissolved and dispersed for rapid absorption in the gastrointestinal tract when administered orally, for example in capsule form. Oral administration is associated with a delayed onset of the desired pharmacological action. It is known that upon oral administration, celecoxib takes approximately 3.0 hours for peak plasma concentrations to be achieved and hence have delayed onset of action after administration. Additionally, the intake of food further influences drug absorption. However, acute pain, as in the case of migraine pain, surgical pain, trauma, pain due to kidney stones, and arthritis, demands immediate or faster pain relief.

Accordingly, there remains an unmet need in the art for compositions of celecoxib or pharmaceutical salts thereof, which provide faster pain relief.

SUMMARY

The present application provides compositions and methods for administering such compositions including celecoxib or pharmaceutical salts thereof, which can be readily dissolved and/or dispersed for rapid absorption in the gastrointestinal tract in order to provide faster pain relief.

Some embodiments disclosed herein provide stable oral liquid pharmaceutical compositions, comprising a therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent, and at least one pharmaceutically acceptable excipient, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 60 min.

In some embodiments, the composition is essentially free of precipitation inhibitors selected from the group consisting of polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer (SOLUPLUS®), polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, and cellulosic polymers, including hydroxypropyl cellulose and hydroxypropyl methylcellulose. In some embodiments, the at least one solubilizer is polyethoxylated castor oil (available as KOLLIPHOR EL®), lauryl macrogolglyceride (available as GELUCIRE® 44/14), or a combination thereof.

In some embodiments, the at least one medium chain glyceride is glyceryl tricaprylate/tricaprate (available as CAPTEX® 300), glyceryl monocaprylate (available as CAPMUL® MCM C8), or a combination thereof. In some embodiments, the at least one polar solvent is selected from the group consisting of propylene glycol, polyethylene glycols having a molecular weight between 400 and 1000, glycerin, C₂ to C₈ mono- and poly-alcohols (e.g., ethanol), C₇ to C₁₈ alcohols of linear or branched configuration, water and mixtures thereof.

In some embodiments, the therapeutically effective amount of celecoxib comprises from about 1% to about 80% celecoxib by weight, based on the total weight of the composition. In some embodiments, the at least one solubilizer is present in an amount of from about 10% to about 70% by weight, based on the total weight of the composition.

In some embodiments, a weight ratio of the at least one solubilizer to celecoxib varies from about 4.0:1.0 to about 20:1.0. In some embodiments, the at least one polar solvent is present in an amount of from about 20% to about 80% by weight, based on the total weight of the composition. In some embodiments, a weight ratio of the at least one solubilizer to the at least one polar solvent varies from about 0.60:1.00 to about 1.8:1.00.

In some embodiments, the at least one medium chain glyceride is present in an amount of from about 5% to about 75% by weight, based on the total weight of the composition. In some embodiments, the composition has a mean oil droplet size of not more than 500 nm, when tested in 250 ml of Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm.

In some embodiments, the composition has a viscosity of from about 20 cps to about 1000 cps. In some embodiments, the composition has a density of from about 0.8 gm/cm³ to about 2 gm/cm³. In some embodiments, the composition has a transmittance of at least 40%. In some embodiments, the composition has a pH of from about 3 to about 7.

In some embodiments, the therapeutically effective amount of celecoxib is at least about 40% less than conventional celecoxib compositions such as CELEBREX® 400 mg oral capsules. In some embodiments, the therapeutically effective amount of celecoxib is about 240 mg. In some embodiments, the therapeutically effective amount of celecoxib is at least about 55% less than conventional celecoxib compositions such as CELEBREX® 400 mg oral capsules. In some embodiments, the therapeutically effective amount of celecoxib is about 180 mg. In some embodiments, the therapeutically effective amount of celecoxib is at least about 70% less than conventional celecoxib compositions such as CELEBREX® 400 mg oral capsules.

In some embodiments, the therapeutically effective amount of celecoxib is about 120 mg. In some embodiments, the stable oral liquid pharmaceutical compositions, which upon oral administration to a human subject under fasting conditions, provides at least one of the following pharmacokinetic parameters:

AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;

AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;

AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;

AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;

AUC_((0-t)) of at least about 2000 ng·h/mL;

AUC_((0-∞)) of at least about 2000 ng·h/mL; and

T_(lag) of not more than 8 minutes.

In some embodiments, the stable oral liquid pharmaceutical compositions comprise: a) a therapeutically effective amount of celecoxib; b) at least one pharmaceutically acceptable excipient; c) at least one solubilizer in an amount from about 35% w/w to about 45% w/w; and d) at least one polar solvent in an amount from about 25% w/w to about 42% w/w, wherein the solubilizer and polar solvent are present in a weight ratio of from about 0.60:1 to about 1.8:1; and wherein the stable oral liquid pharmaceutical composition has a viscosity of from about 20 cps to about 1000 cps, and a density of from about 0.8 gm/cm³ to about 2 gm/cm³.

Some embodiments disclosed here provide stable oral liquid pharmaceutical compositions comprising from about 100 mg to 250 mg of celecoxib, at least one pharmaceutically acceptable excipient, at least one solubilizer, at least one medium chain glyceride, and at least one polar solvent, wherein the composition: a) releases no less than about 70% of the celecoxib at a period of 10 minutes; or b) releases no less than about 80% of the celecoxib at a period of 15 minutes, in 900 ml of 0.01N HCl with 0.5% sodium lauryl sulfate, when tested in a USP Type 2 apparatus with sinkers at 50 rpm and 37° C.

In some embodiments, the composition is essentially free of precipitation inhibitors selected from the group consisting of polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer (SOLUPLUS®), polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, and cellulosic polymers, including hydroxypropyl cellulose and hydroxypropyl methylcellulose. In some embodiments, the at least one solubilizer is polyethoxylated castor oil (available as KOLLIPHOR EL®), lauryl macrogolglyceride (available as GELUCIRE® 44/14), or a combination thereof. In some embodiments, the at least one medium chain glyceride is glyceryl tricaprylate/tricaprate (available as CAPTEX® 300), glyceryl monocaprylate (available as CAPMUL® MCM C8), or a combination thereof.

In some embodiments, the at least one polar solvent is selected from the group consisting of propylene glycol, polyethylene glycols having a molecular weight between 400 and 1000, glycerin, C₂ to C₈ mono- and poly-alcohols (e.g., ethanol), C₇ to C₁₈ alcohols of linear or branched configuration, water and mixtures thereof.

In some embodiments, the therapeutically effective amount of celecoxib comprises from about 1% to about 80% celecoxib by weight, based on the total weight of the composition. In some embodiments, the at least one solubilizer is present in an amount of from about 10% to about 70% by weight, based on the total weight of the composition. In some embodiments, a weight ratio of the at least one solubilizer to celecoxib varies from about 4.0:1.0 to about 20:1.0.

In some embodiments, the at least one polar solvent is present in an amount of from about 20% to about 80% by weight, based on the total weight of the composition. In some embodiments, a weight ratio of the at least one solubilizer to the at least one polar solvent varies from about 0.60:1.00 to about 1.8:1.00.

In some embodiments, the at least one medium chain glyceride is present in an amount of from about 5% to about 75% by weight, based on the total weight of the composition. In some embodiments, the composition has a mean oil droplet size of not more than 500 nm, when tested in 250 ml of Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm.

In some embodiments, the composition has a viscosity of from about 20 cps to about 1000 cps. In some embodiments, the composition has a density of from about 0.8 gm/cm³ to about 2 gm/cm³. In some embodiments, the composition has a transmittance of at least 40%. In some embodiments, the composition has a pH of from about 3 to about 7.

In some embodiments, the therapeutically effective amount of celecoxib is at least about 40% less than conventional celecoxib compositions such as CELEBREX® 400 mg oral capsules. In some embodiments, the therapeutically effective amount of celecoxib is about 240 mg. In some embodiments, the therapeutically effective amount of celecoxib is at least about 55% less than conventional celecoxib compositions such as CELEBREX® 400 mg oral capsules. In some embodiments, the therapeutically effective amount of celecoxib is about 180 mg. In some embodiments, the therapeutically effective amount of celecoxib is at least about 70% less than conventional celecoxib compositions such as CELEBREX® 400 mg oral capsules. In some embodiments, the therapeutically effective amount of celecoxib is about 120 mg.

In some embodiments, the stable oral liquid pharmaceutical compositions, which upon oral administration to a human subject under fasting conditions, provides at least one of the following pharmacokinetic parameters:

AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;

AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;

AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;

AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;

AUC_((0-t)) of at least about 2000 ng·h/mL;

AUC_((0-∞)) of at least about 2000 ng·h/mL; and

T_(lag) of not more than 8 minutes.

In some embodiments, the stable oral liquid pharmaceutical compositions comprise: a) a therapeutically effective amount of celecoxib; b) at least one pharmaceutically acceptable excipient; c) at least one solubilizer in an amount from about 35% w/w to about 45% w/w; and d) at least one polar solvent in an amount from about 25% w/w to about 42% w/w, wherein the solubilizer and polar solvent are present in a weight ratio of from about 0.60:1 to about 1.8:1; and wherein the stable oral liquid pharmaceutical composition has a viscosity of from about 20 cps to about 1000 cps, and a density of from about 0.8 gm/cm³ to about 2 gm/cm³.

Some embodiments disclosed herein provide methods of treating pain in a human subject, the method comprising administering to the subject a stable oral liquid pharmaceutical composition, comprising a therapeutically effective amount of celecoxib, at least one solubilizer in amount from about 35 w/w to about 45 w/w, at least one polar solvent in amount from about 25% w/w to about 42% w/w, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, wherein the stable oral liquid pharmaceutical composition is essentially free of precipitation inhibitors.

In some embodiments, the pain is associated with migraine. In some embodiments, the therapeutically effective amount of celecoxib is sufficient to render the subject pain free within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, the therapeutically effective amount of celecoxib is sufficient to lead to partial pain relief in the subject within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to freedom from pain at 2 hours following administration in at least 25% of the treated human subjects. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to partial pain relief at 2 hours following administration in at least 45% of the treated human subjects.

In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being pain free at 2 hours following administration, which is at least 40% greater in comparison to the percentage of human subjects being treated with a placebo. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being partially relieved of pain at 2 hours following administration, which is at least 10% greater in comparison to the percentage of human subjects being treated with a placebo. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being pain free at 2 hours following administration, which is at least 10% greater in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg). In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being partially relieved of pain at 2 hours following administration, which is at least 10% greater in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg).

In some embodiments disclosed herein the methods for providing pain freedom in a human subject suffering from pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib. In some embodiments disclosed herein the methods for providing pain freedom in a human subject suffering from pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib.

In some embodiments disclosed herein the methods for providing pain freedom at 2 hours following administration in a human subject suffering from pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib. In some embodiments disclosed herein the methods for providing pain freedom at 2 hours following administration in a human subject suffering from pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib.

In some embodiments, the method for providing partial pain relief in less than about 2 hours following administration in a human subject suffering from a pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib. In some embodiments, the method for providing partial pain relief in less than about 2 hours following administration in a human subject suffering from a pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib.

In some embodiments, the method for providing partial pain relief in less than about 2 hours following administration in a human subject suffering from a pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said partial pain relief is maintained for at least about 4 hours. In some embodiments, the method for providing partial pain relief in less than about 2 hours following administration in a human subject suffering from a pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said partial pain relief is maintained for at least about 4 hours.

In some embodiments, the method for providing partial pain relief in less than about 2 hours following administration in a human subject suffering from a pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said partial pain relief is ≥1 level lower pain intensity reported by the human subject suffering from pain, than the predose rating on a 4-point numeric rating scale for pain with a range of 0 (no pain) to 3 (severe). In some embodiments, the method for providing partial pain relief in less than about 2 hours in a human subject suffering from a pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said partial pain relief is ≥1 level lower pain intensity reported by the human subject suffering from pain, than the predose rating on a numeric rating scale for pain with a range of 0 (no pain) to 3 (severe).

In some embodiments disclosed herein the method for providing pain freedom in a human subject suffering from pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein the pain freedom is maintained for at least about 2 hours to about 24 hours. In some embodiments disclosed herein the method for providing pain freedom in a human subject suffering from pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said pain freedom is maintained for at least about 2 hours to about 24 hours.

In some embodiments, the method for reducing the most bothersome symptoms in a human subject suffering from migraine involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said most bothersome symptoms are reduced within about 2 hours of administration of said composition. In some embodiments, the method for reducing the most bothersome symptoms in a human subject suffering from migraine involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said most bothersome symptoms are reduced within about 2 hours of administration of said composition.

In an aspect of the above embodiment, the method maintains the freedom from most bothersome symptoms associated with migraine for at least about 2 hours to about 24 hours. In some embodiments, the method for reducing the most bothersome symptoms in a human subject suffering from migraine involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said method maintains the freedom from most bothersome symptoms associated with migraine for at least about 2 hours to about 24 hours.

Some embodiments disclosed herein provide uses of a stable oral liquid pharmaceutical composition disclosed in any of the embodiments throughout this application for the treatment of pain in a subject. In some embodiments, the stable oral liquid pharmaceutical composition comprises a therapeutically effective amount of celecoxib, at least one solubilizer in amount from about 35 w/w to about 45 w/w, at least one polar solvent in amount from about 25% w/w to about 42% w/w, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, wherein the stable oral liquid pharmaceutical composition is essentially free of precipitation inhibitors. In some embodiments, the pain is associated with migraine.

In some embodiments, the therapeutically effective amount of celecoxib is sufficient to render the subject pain free within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, the therapeutically effective amount of celecoxib is sufficient to lead to partial pain relief in the subject within 2 hours of administering the stable oral liquid pharmaceutical composition.

In some embodiments, administering the stable oral liquid pharmaceutical composition leads to pain free at 2 hours in at least 25% of the treated human subjects. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to partial pain relief at 2 hours in at least 45% of the treated human subjects. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being pain free at 2 hours that is at least 40% in comparison to the percentage of human subjects being treated with a placebo. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being partially relieved of pain at 2 hours that is at least 10% in comparison to the percentage of human subjects being treated with a placebo.

In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being pain free at 2 hours that is at least 10% in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg). In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being partially relieved of pain at 2 hours that is at least 10% in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg).

Some embodiments disclosed herein provide stable oral liquid pharmaceutical compositions of celecoxib comprising (i) therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride; and (ii) polar solvent comprising mixture of ethanol and glycerin; wherein the composition falls within the shaded region of a phase diagram, as shown in Figure. 1, wherein boundaries of a stable composition are defined by shaded region or the region between the connecting lines between the six points (a, b, c, d, e and f), wherein the composition comprises about 1% to about 80% w/w celecoxib and correspond to a weight % ratio of base composition:ethanol:glycerin of 0.200:0.024:0.712 for a, 0.200:0.376:0.360 for b, 0.200:0.400:0.336 for c, 0.536:0.400:0.000 for d, 0.900:0.036:0.00 for e, and 0.900:0.00:0.036 for f.

In some embodiments, said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 60 min. In some embodiments, the composition is essentially free of precipitation inhibitors selected from the group consisting of polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer (SOLUPLUS®), polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, and cellulosic polymers, including hydroxypropyl cellulose and hydroxypropyl methylcellulose. In some embodiments, the at least one solubilizer is polyethoxylated castor oil (available as KOLLIPHOR EL®), lauryl macrogolglyceride (available as GELUCIRE® 44/14), or a combination thereof. In some embodiments, the at least one medium chain glyceride is glyceryl tricaprylate/tricaprate (available as CAPTEX® 300), glyceryl monocaprylate (available as CAPMUL® MCM C8), or a combination thereof.

In some embodiments, the at least one polar solvent is selected from the group consisting of propylene glycol, polyethylene glycols having a molecular weight between 400 and 1000, glycerin, C₂ to C₈ mono- and poly-alcohols (e.g., ethanol), C₇ to C₁₈ alcohols of linear or branched configuration, water and mixtures thereof.

In some embodiments, the therapeutically effective amount of celecoxib comprises from about 1% to about 80% celecoxib by weight, based on the total weight of the composition.

In some embodiments, the at least one solubilizer is present in an amount of from about 10% to about 70% by weight, based on the total weight of the composition. In some embodiments, a weight ratio of the at least one solubilizer to celecoxib varies from about 4.0:1.0 to about 20:1.0. In some embodiments, the at least one polar solvent is present in an amount of from about 20% to about 80% by weight, based on the total weight of the composition. In some embodiments, a weight ratio of the at least one solubilizer to the at least one polar solvent varies from about 0.60:1.00 to about 1.8:1.00.

In some embodiments, the at least one medium chain glyceride is present in an amount of from about 5% to about 75% by weight, based on the total weight of the composition. In some embodiments, the composition has a mean oil droplet size of not more than 500 nm, when tested in 250 ml of Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm. In some embodiments, the composition has a viscosity of from about 20 cps to about 1000 cps. In some embodiments, the composition has a density of from about 0.8 gm/cm³ to about 2 gm/cm³. In some embodiments, the composition has a transmittance of at least 40%. In some embodiments, the composition has a pH of from about 3 to about 7.

In some embodiments, the therapeutically effective amount of celecoxib is at least about 40% less than conventional celecoxib compositions such as CELEBREX® 400 mg oral capsules. In some embodiments, the therapeutically effective amount of celecoxib is about 240 mg. In some embodiments, the therapeutically effective amount of celecoxib is at least about 55% less than conventional celecoxib compositions such as CELEBREX® 400 mg oral capsules. In some embodiments, the therapeutically effective amount of celecoxib is about 180 mg. In some embodiments, the therapeutically effective amount of celecoxib is at least about 70% less than conventional celecoxib compositions such as CELEBREX® 400 mg oral capsules. In some embodiments, the therapeutically effective amount of celecoxib is about 120 mg.

In some embodiments, the stable oral liquid pharmaceutical compositions, which upon oral administration to a human subject under fasting conditions, provides at least one of the following pharmacokinetic parameters:

AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;

AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;

AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;

AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;

AUC_((0-t)) of at least about 2000 ng·h/mL;

AUC_((0-∞)) of at least about 2000 ng·h/mL; and

T_(lag) of not more than 8 minutes.

In some embodiments, the stable oral liquid pharmaceutical compositions comprise: a) a therapeutically effective amount of celecoxib; b) at least one pharmaceutically acceptable excipient; c) at least one solubilizer in an amount from about 35% w/w to about 45% w/w; and d) at least one polar solvent in an amount from about 25% w/w to about 42% w/w, wherein the solubilizer and polar solvent are present in a weight ratio of from about 0.60:1 to about 1.8:1; and wherein the stable oral liquid pharmaceutical composition has a viscosity of from about 20 cps to about 1000 cps, and a density of from about 0.8 gm/cm³ to about 2 gm/cm³.

Some embodiments disclosed herein provide methods of treating pain in a human subject, the method comprising administering to the subject a stable oral liquid pharmaceutical composition, comprising a therapeutically effective amount of celecoxib, at least one solubilizer, at least one polar solvent, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, wherein the stable oral liquid pharmaceutical composition is essentially free of precipitation inhibitors, wherein the therapeutically effective amount of celecoxib is sufficient to render the subject pain free lasting for at least 24 hours after administering the stable oral liquid pharmaceutical composition.

In some embodiments, the stable oral liquid pharmaceutical composition comprises a therapeutically effective amount of celecoxib, at least one solubilizer in amount from about 35% w/w to about 45% w/w, at least one polar solvent in amount from about 25% w/w to about 42% w/w, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, wherein the stable oral liquid pharmaceutical composition is essentially free of precipitation inhibitors.

In some embodiments, the pain is associated with migraine. In some embodiments, the therapeutically effective amount of celecoxib is sufficient to render the subject pain free within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, the therapeutically effective amount of celecoxib is sufficient to lead to partial pain relief in the subject within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to pain free lasting for at least 24 hours after treatment in at least 25% of the treated human subjects. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to pain free lasting for at least 24 hours after treatment in at least 45% of the treated human subjects. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being pain free lasting for at least 24 hours after treatment that is at least 40% in comparison to the percentage of human subjects being treated with a placebo. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being pain free lasting for at least 24 hours after treatment that is at least 10% in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg).

Some embodiments disclosed herein provide methods of treating pain in a human subject, the method comprising administering to the subject a stable oral liquid pharmaceutical composition, comprising a therapeutically effective amount of celecoxib, at least one solubilizer, at least one polar solvent, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, wherein the stable oral liquid pharmaceutical composition is essentially free of precipitation inhibitors, provides at least 30%, at least 40% or at least 50% of the human subjects are free of any Most Bothersome Symptom at 2 hours.

Some embodiments disclosed herein provide methods of treating pain in a human subject, the method comprising administering to the subject a stable oral liquid pharmaceutical composition, comprising a therapeutically effective amount of celecoxib, at least one solubilizer, at least one polar solvent, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, wherein the stable oral liquid pharmaceutical composition is essentially free of precipitation inhibitors, wherein the therapeutically effective amount of celecoxib is sufficient to render the subject free of most bothersome symptoms within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, the stable oral liquid pharmaceutical composition comprises a therapeutically effective amount of celecoxib, at least one solubilizer in amount from about 35% w/w to about 45% w/w, at least one polar solvent in amount from about 25% w/w to about 42% w/w, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, wherein the stable oral liquid pharmaceutical composition is essentially free of precipitation inhibitors. In some embodiments, the pain is associated with migraine.

In some embodiments, the therapeutically effective amount of celecoxib is sufficient to render the subject pain free within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, the therapeutically effective amount of celecoxib is sufficient to lead to partial pain relief in the subject within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to free of most bothersome symptoms within 2 hours of treatment in at least 25% of the treated human subjects. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to free of most bothersome symptoms within 2 hours of treatment in at least 45% of the treated human subjects. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being free of most bothersome symptoms within 2 hours of treatment that is at least 40% in comparison to the percentage of human subjects being treated with a placebo. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being free of most bothersome symptoms within 2 hours of treatment that is at least 10% in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg).

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a ternary phase diagram. The shaded region is “stable composition region A” and is formed by connecting lines between points (a, b, c, d, e, and f).

FIG. 2 shows a ternary phase diagram. The shaded region is “stable composition region B” and is formed by connecting lines between points (a, b, c, d, e, and f).

FIG. 3 shows a ternary phase diagram. The shaded region is “stable composition region C” and is formed by connecting lines between points (a, b, c, d, e, f, g, and h).

FIG. 4 shows pain free in percentage of human subjects at 2 hours results of the Example 3 having 120 mg Celecoxib (Treatment-1) compared to VIOXX 25, VIOXX 50 & CAMBIA 50.

FIG. 5 shows percentage pain relief in percentage of human subjects at 2 hours results of the Example 3 having 120 mg Celecoxib (Treatment-1) compared to VIOXX 25, VIOXX 50 & CAMBIA 50.

FIG. 6 shows pain free in percentage of human subjects at 2 hours and pain free at 24 hours results of the Example 3 having 120 mg Celecoxib (Treatment-1) compared to VIOXX 25, VIOXX 50 & CAMBIA 50.

FIG. 7 shows most bothersome symptom (MBS) free in percentage of human subjects at 2 hours following the administration of the Example 3 having 120 mg Celecoxib (Treatment-1).

DETAILED DESCRIPTION OF EMBODIMENTS OF THE INVENTION

Definitions

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art.

As used herein, “comprising” is open-ended and means the elements recited, or their equivalent in structure or function, plus any other element or elements which are not recited. The terms ‘having” and “including” are also to be construed as open-ended unless the context suggests otherwise.

All the ranges recited herein include the endpoints, including those that recite a range “between” two values. As an illustration, a numerical range of 1 to 5 should be interpreted to include not only the explicitly recited values of 1 to 5, but also include individual values and sub-ranges within the indicated range. Thus, included in this numerical range are individual values such as 2, 3, and 4 and sub-ranges such as from 1-3, from 2-4, and from 3-5, etc., as well as 1, 2, 3, 4, or 5, individually. This same principle applies to ranges reciting only one numerical value as a minimum or a maximum.

The terms “a” and “the” as used herein are understood to encompass the plural as well as the singular. For example, reference to “an excipient” includes reference to one or more of such excipients, and reference to “the carrier” includes reference to one or more of such carriers.

The terms such as “about,” “up to,” “generally,” “substantially” and the like are to be construed as modifying a term or value such that it is not an absolute. Such terms will be defined by the circumstances and the terms that they modify as those terms are understood by those of skilled in the art. The terms are indicative of an approximation or some amount of deviation, rather than perfect and absolute. The terms include, at very least, the degree of expected experimental error, technical error, and instrumental error for a given experiment, technique or an instrument used to measure a value. The terms can refer to a higher tolerance of variation depending on, for instance, the experimental technique used. Said variations of a specified value are understood by the skilled person and are within the context of the present invention.

As used herein, “free of” a particular compound or compositions or excipients refer to the absence of any separately added portion of the referenced compound or composition or excipients. The term “essentially free of” means that there is less than 1% w/w of a particular compound or compositions, or excipients, wherein the amount present does not impart any functional value to the composition.

“Celecoxib” as used herein encompasses base form as well as its pharmaceutically acceptable salts, complexes, polymorphs, hydrates, solvates, enantiomers or racemates. The solid state form of celecoxib used in the composition of the present application is not critical. For example, celecoxib can be amorphous or crystalline.

The term “pharmaceutically acceptable salts” as used herein includes those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, which are well known in the art. The salts can be prepared in situ during the final isolation and purification of the compounds of the invention, or separately by reacting the pharmaceutically active substance, having a freebase function, with a suitable organic acid or inorganic acid.

As used herein, an “effective amount” or a “therapeutically effective amount” of a drug refers to a non-toxic, but sufficient amount of the drug, to achieve therapeutic results in treating a condition for which the drug is known to be effective. In this instance, an effective amount is an amount of celecoxib which is sufficient to treat pain in a patient in need thereof which is to say to provide some measure of analgesia to reduce at least the patient's perception of pain.

The term “liquid composition” refers to a liquid composition that is ingested with or without further mixing with aqueous or suitable media before oral administration.

The term “stable composition(s)” as used herein, refers to a composition that does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes. Also the term “stable composition(s)” refers to a composition which upon subjected to stability evaluation at 40° C. and 75% RH (relative humidity) or 25° C. and 60% RH (relative humidity), is substantially free of impurities, or comprises not more than 5% impurities, or comprises impurities levels which are acceptable by regulatory bodies such as US FDA.

The term “precipitation inhibitor” as used herein refers to a pharmaceutically acceptable excipient that prevents the precipitation of celecoxib when orally administered to a human subject, or when tested in a simulated gastric fluid, e.g., Fasted-State Simulated Gastric Fluid (FaSSGF), pH 2.0, at 37° C. under stirring condition. Examples of precipitation inhibitors include: polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer (SOLUPLUS®), polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, and cellulosic polymers, including hydroxypropyl cellulose and hydroxypropyl methylcellulose. Non-cellulosic polymers that inhibit precipitation may also be included among the possible precipitation inhibitors.

The term “Fasted-State Simulated Gastric Fluid (FaSSGF)” as used herein, refers to a standard in vitro assay that is used to simulate the environment of the fasted-state gastric fluid for evaluation of the stability (or solubility or suitability) of drug formulations for oral delivery. The composition of FaSSGF is 0.1N HCl with 0.05% SLS and pH adjusted with NaOH/HCl.

The term “conventional celecoxib oral composition” or “conventional composition” as used herein, refers to oral celecoxib capsules marketed under the brand name CELEBREX® by G.D. Searle LLC in US or its pharmaceutical equivalents or its therapeutic equivalents or later approved drugs which are designated as AB rated by US FDA as per Approved Drug Products with Therapeutic Equivalence Evaluations (34th edition) or drugs obtained marketing approval by US FDA through Abbreviated New Drug Application (ANDA) filing by establishing bioequivalence to such Product”. In some embodiments CELEBREX® includes its US FDA approved therapeutic or pharmaceutical equivalents. CELEBREX® is a Trademark registered and owned by G.D. Searle LLC (Division of Pfizer Inc. NY), NY 10017, USA. In some other embodiments “conventional celecoxib oral composition” or “conventional composition” also includes oral celecoxib capsules marketed under the brand name ZYCEL® by Zydus Cadila, Zydus Tower, Ahmedabad, India. CELEBREX® is available in the strengths of 50 mg, 100 mg, 200 mg and 400 mg celecoxib containing oral capsules. ZYCEL® is available in the strengths of 100 mg and 200 mg celecoxib containing oral capsules.

As used herein the term “pain” refers to pain as recited herein acute pain, migraine pain, cluster headache, neuropathic pain, post-operative pain, chronic lower back pain, herpes neuralgia, phantom limb pain, central pain, dental pain, neuropathic pain, opioid-resistant pain, visceral pain, surgical pain, bone injury pain, pain during labor and delivery, pain resulting from burns, including sunburn, post-partum pain, angina pain, and genitourinary tract-related pain including cystitis, arthritis pain, inflammation, osteoarthritis, juvenile rheumatoid arthritis, ankylosing spondylitis, primary dysmenorrhea, breakthrough pain, or any kind of cancer pain.

As used herein the term “treating” includes treatment and/or prophylaxis of a physical and/or mental condition or amelioration or elimination of the developed condition once it has been established or alleviation of the characteristic symptoms of such condition.

As used herein, the term “mammal” shall refer to the mammalian class of higher vertebrates. The term “mammal” includes, but is not limited to, a human.

As used herein the term “pain freedom” or “pain free” refers to a patient report of no pain on a numeric rating scale for pain with a range of 0 (no pain) to 3 (severe pain), as per “Guidelines for controlled trials of drugs in migraine: Third edition. A guide for investigators” Tfelt-Hansen P, Pascual J, Ramadan N, et al. Cephalalgia, 2012; 32(1):6-38.

As used herein the term “headache pain relief” or “partial pain relief” or “partially relieved” or “pain relief” refers to a patient report of pain intensity ≥1 level lower than the predose rating on a numeric rating scale for pain with a range of 0 (no pain) to 3 (severe pain), as per “Guidelines for controlled trials of drugs in migraine: Third edition. A guide for investigators” Tfelt-Hansen P, Pascual J, Ramadan N, et al. Cephalalgia, 2012; 32(1):6-38.

When the term “maintained” is used herein in connection with pain freedom or pain relief for a period of time, the period is measured from the onset of the pain freedom pain relief. For example, if pain freedom is maintained for at least about 2 hours, the period of time is measured from the time point following administration at which the patient experiences no pain. As such, if the patient experiences pain freedom at 2 hours following administration, then the period of time that pain freedom is maintained is measured from the time point of 2 hours following administration.

In addition to “pain” or “headache pain” experienced by a patient suffering from migraine, the patient typically suffers from other “most bothersome symptoms,” which are unique to the patient and based on a patient report that identifies such most bothersome symptoms, as is understood in the art. Such symptoms include, but are not necessarily limited to nausea, vomiting, photophobia (light sensitivity), and phonophobia (sound sensitivity). Other examples of such symptoms include, but are not limited to, sensitivity to smell, sensitivity to touch, blurred vision and other visual phenomena, lightheadedness, fainting, vertigo, dizziness, and mood changes.

Stable Oral liquid Pharmaceutical Compositions

In some embodiments, the present application provides stable oral liquid pharmaceutical compositions comprising a therapeutically effective amount of celecoxib. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein comprise at least one solubilizer, at least one medium chain glyceride, at least one polar solvent, and/or at least one pharmaceutically acceptable excipient.

Without being bound by a particular theory, it is contemplated that the stable oral liquid pharmaceutical compositions disclosed herein show improved solubilization characteristics, for example, when administered orally to a human subject. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein do not show any precipitation in a simulated gastric fluid (SGF) for a prolonged time. For example, the stable oral liquid pharmaceutical compositions disclosed herein do not show any precipitation in a simulated gastric fluid (SGF) for at least 10 min, at least 20 min, at least 30 min, at least 40 min, at least 50 min, at least 60 min, at least 90 min, at least 2 hr, at least 3 hr, at least 4 hr, at least 5 hr, at least 6 hr, at least 12 hr, at least 24 hr, or longer. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein do not show any precipitation in a Fasted-State Simulated Gastric Fluid (FaSSGF) for a prolonged time. For example, the stable oral liquid pharmaceutical compositions disclosed herein do not show any precipitation in a Fasted-State Simulated Gastric Fluid (FaSSGF) for at least 10 min, at least 20 min, at least 30 min, at least 40 min, at least 50 min, at least 60 min, at least 90 min, at least 2 hr, at least 3 hr, at least 4 hr, at least 5 hr, at least 6 hr, at least 12 hr, at least 24 hr, or longer.

In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein do not show any precipitation in a low pH environment. For example, the stable oral liquid pharmaceutical compositions disclosed herein do not show any precipitation in a Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 1.0-6.0 for at least 10 min, at least 20 min, at least 30 min, at least 40 min, at least 50 min, at least 60 min, at least 90 min, at least 2 hr, at least 3 hr, at least 4 hr, at least 5 hr, at least 6 hr, at least 12 hr, at least 24 hr, or longer. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein do not show any precipitation in a Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 1.0-5.0 for at least 10 min, at least 20 min, at least 30 min, at least 40 min, at least 50 min, at least 60 min, at least 90 min, at least 2 hr, at least 3 hr, at least 4 hr, at least 5 hr, at least 6 hr, at least 12 hr, at least 24 hr, or longer. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein do not show any precipitation in a Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 1.0-4.0 for at least 10 min, at least 20 min, at least 30 min, at least 40 min, at least 50 min, at least 60 min, at least 90 min, at least 2 hr, at least 3 hr, at least 4 hr, at least 5 hr, at least 6 hr, at least 12 hr, at least 24 hr, or longer. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein do not show any precipitation in a Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 1.0-3.0 for at least 10 min, at least 20 min, at least 30 min, at least 40 min, at least 50 min, at least 60 min, at least 90 min, at least 2 hr, at least 3 hr, at least 4 hr, at least 5 hr, at least 6 hr, at least 12 hr, at least 24 hr, or longer. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein do not show any precipitation in a Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0-3.0 for at least 10 min, at least 20 min, at least 30 min, at least 40 min, at least 50 min, at least 60 min, at least 90 min, at least 2 hr, at least 3 hr, at least 4 hr, at least 5 hr, at least 6 hr, at least 12 hr, at least 24 hr, or longer. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein do not show any precipitation in a Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0 for at least 10 min, at least 20 min, at least 30 min, at least 40 min, at least 50 min, at least 60 min, at least 90 min, at least 2 hr, at least 3 hr, at least 4 hr, at least 5 hr, at least 6 hr, at least 12 hr, at least 24 hr, or longer.

Without being bound by any particular theory, the stable oral liquid pharmaceutical compositions disclosed herein are essentially free of any precipitation inhibitors. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein are completely free of any precipitation inhibitors. In some embodiments, the celecoxib composition of present application is essentially free of precipitation inhibitors such as polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose, and hydroxypropyl methylcellulose. In some embodiments, the celecoxib compositions of the present application are essentially free of precipitation inhibitors including polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer (SOLUPLUS®), polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, cellulosic polymers, including hydroxypropyl cellulose and hydroxypropyl methylcellulose, and non-cellulosic polymers.

In some embodiments, the present application provides a stable oral pharmaceutical composition comprising therapeutically effective amount of celecoxib, wherein said composition provides mean oil droplet size of no more than 500 nm, when tested in 250 ml of Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm.

In some embodiments, the present application provides a stable oral pharmaceutical composition comprising therapeutically effective amount of celecoxib, wherein said composition does not show any precipitation in the dissolution medium or Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 30 min or 60 min or 90 min or 120 min or 180 min or 240 min time points; and said composition is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In some embodiments, the present application provides a stable oral liquid pharmaceutical composition comprising therapeutically effective amount of celecoxib, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 30 min or 60 min or 90 min or 120 min or 180 min or 240 min time points; and said composition is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In some embodiments, the present application provides a stable oral pharmaceutical composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 30 min or 60 min or 90 min or 120 min or 180 min or 240 min time points; and said composition is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In some embodiments, the present application provides a stable oral liquid pharmaceutical composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipients, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 30 min or 60 min or 90 min or 120 min or 180 min or 240 min time points; and said composition is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

The oral pharmaceutical celecoxib composition of present application can be formulated in the form of a solution, suspension, emulsion or liquid mixture.

Medium Chain Glycerides

In some embodiments, the stable oral liquid pharmaceutical compositions of the present application further comprise at least one medium chain glycerides. As used herein, a medium chain glyceride can refer to a medium chain mono-glyceride, a medium chain bi-glyceride, and/or a medium chain triglyceride (MCT). MCTs are triglycerides whose fatty acids have an aliphatic tail of 6-12 carbon atoms. MCTs are composed of a glycerol backbone and three fatty acids. In the case of MCTs, 2 or 3 of the fatty acid chains attached to glycerol are medium-chain in length. Exemplary medium chain fatty acids include Caproic acid, Caprylic acid, Capric acid, Lauric acid, etc. It would be appreciated that the medium chain glycerides, such as MCTs, can improve the solubility of the stable oral liquid pharmaceutical compositions disclosed herein when orally administered to the human subject, or in a simulated gastric fluid, e.g., Fasted-State Simulated Gastric Fluid (FaSSGF).

The medium chain glyceride may be present in the stable oral liquid pharmaceutical compositions disclosed herein in a variety of concentrations. For example, the stable oral liquid pharmaceutical compositions disclosed herein can comprise a medium chain glyceride of at least 10% by weight, at least 20% by weight, at least 30% by weight, at least 40% by weight, at least 50% by weight, at least 60% by weight, at least 70% by weight, at least 80% by weight, at least 90% by weight, or a percentage between any two of the above values, based on the total weight of the composition.

In some embodiments, the celecoxib compositions of present application comprises of at least one medium chain glyceride in an amount of from about 5% to about 75% by weight, or from about 5% to about 65% by weight, or from about 5% to about 55% by weight, or from about 5% to about 45% by weight, or from about 5% to about 35% by weight, based on the total weight of the composition.

In some embodiments, the celecoxib compositions of present application further comprises of medium chain glycerides having at least one medium chain mono- or di- or tri-glyceride or mixtures thereof.

Suitable examples of medium chain mono- or di or tri-glyceride (MCT) used in the compositions of the present application are well known in the art. The non-limiting examples of medium chain mono- or di or tri-glyceride (MCT) include, but are not limited to, both even and odd fatty acids, such as fatty acids containing C4 (butyric acid, butanoic acid), C5 (valeric acid), C6 (caproic acid, hexanoic acid), C7 (heptanoic acid), C8 (caprylic acid, octanoic acid), C9 (pelargonic acid), C10 (capric acid, decanoic acid), C11 (undecanoic acid) or C12 (lauric acid, dodecanoic acid) and both even and odd fatty acid (containing two to twelve carbon atoms) ester with glycerol such as glyceryl monocaprylate, glyceryl di-caprylate, propylene glycol heptanoate, glyceryl monocaprate, glyceryl caprylate/caprate, medium chain mono- and diglycerides available as CAPMUL MCM®, propylene glycol monocaprylate and di-caprylate, glyceryl tricaprylate, glycerol tricaprylate/caprate, glyceryl tricaprylate/tricaprate, glyceryl tricaprylate/tricaprate PEG-8 Caprylic/Capric Glycerides. Further the medium chain glyceride component may be a naturally occurring mono- or di or tri-glycerides containing composition, such as obtained from butterfat, soy oil, coconut oil and the like.

In some embodiments, the celecoxib compositions of present application comprises of at least one medium chain glycerides selected from the group of Lauroyl macrogolglycerides, Glyceryl Monocaprylate, Glyceryl Tricaprylate/Tricaprate or mixtures thereof.

Alternatively, said glyceride component may comprise at least one industrially prepared glyceride or a mixture of naturally occurring and industrially prepared glycerides. Said glyceride may be prepared by interesterification of C4 to C12 chain fatty acids such as caprylocaproyl macrogol-8 glycerides.

Polar Solvents

In some embodiments, the stable oral liquid pharmaceutical compositions of the present application further comprise at least one polar solvent. Without being bound by any particular theory, the addition of polar solvent in the compositions of celecoxib as per present application additionally helps in delaying the onset of precipitation time. In some embodiments, the onset of precipitation is delayed at least about 1-10 hours compared to the compositions of celecoxib which are substantially free of polar solvent. In some embodiments, the polar solvent can delay the onset of precipitation time for at least about 1 hour, at least about 2 hours, at least about 3 hours, at least about 4 hours, at least about 5 hours, at least about 6 hours, or more.

Suitable examples of polar solvent that can be used in the present application are selected from the group comprising propylene glycol, polyethylene glycols having a molecular weight between 400 and 1000, glycerin, C₂ to C₈ mono- and poly-alcohols such as ethanol, etc., C₇ to C₁₈ alcohols of linear or branched configuration, water and any combination thereof.

The polar solvent may be present in the stable oral liquid pharmaceutical compositions disclosed herein in a variety of concentrations. For example, the stable oral liquid pharmaceutical compositions disclosed herein can comprise a polar solvent of at least 10% by weight, at least 20% by weight, at least 30% by weight, at least 40% by weight, at least 50% by weight, at least 60% by weight, at least 70% by weight, at least 80% by weight, at least 90% by weight, or a percentage between any two of the above values, based on the total weight of the composition.

In some embodiments, the celecoxib compositions of present application comprises of polar solvent in an amount of from about 20% to about 80% by weight, or from about 20% to about 70% by weight, or from about 20% to about 60% by weight, or from about 20% to about 50% by weight, or from about 20% to about 40% by weight, based on the total weight of the composition.

Solubilizers

In some embodiments, the stable oral liquid pharmaceutical compositions of the present application comprises of at least one solubilizer selected from the group of nonionic, anionic, cationic and zwitterionic surfactants or mixtures thereof.

Suitable non-limiting examples of the solubilizer(s) used in the compositions of the present application includes, but not limited to, polyethoxylated fatty acids like esters of lauric acid, oleic acid, and stearic acid, PEG-fatty acid diesters like PEG-20 dilaurate, PEG-fatty acid mono- and di-ester mixtures, alcohol-oil transesterification products like PEG-35 castor oil, Polyoxyl 35 castor oil, polyoxyl 40 hydrogenated castor oil, etc., polyglycerized fatty acids like polyglyceryl oleate, etc., propylene glycol fatty acid esters like propylene glycol monolaurate etc, mixtures of propylene glycol esters-glycerol esters like oleic acid esters of propylene glycol and glycerol, etc., sterol and sterol derivatives like PEG-24 cholesterol ether etc, polyethylene glycol sorbitan fatty acid esters like PEG-20 sorbitan monolaurate etc, polyethylene glycol alkyl ethers like PEG-3 oleyl ether, etc., sugar esters like sucrose monopalmitate etc, polyethylene glycol alkyl phenols like Octoxynol-1 etc, sorbitan fatty acid esters like sorbitan monolaurate, lower alcohol fatty acid esters like ethyl oleate, etc., anionic surfactants include fatty acid salts and bile salts. Additional exemplary solubilisers include, but are not limited to: polyoxyethylene alkylethers; polyethylene glycol fatty acid esters; polyethylene glycol glycerol fatty acid esters; polyoxyethylene sorbitan fatty acid esters; polyglycerol fatty acid esters; polyoxyethylene glycerides; polyoxyethylene vegetable oils; polyoxyethylene hydrogenated vegetable oils, alkylglucosides; alkylmaltosides; alkylthioglucosides; lauryl macrogolglycerides. Ionic surfactants include sodium oleate, sodium lauryl sulfate, sodium lauryl sarcosinate, sodium dioctyl sulfosuccinate, sodium cholate, and sodium taurocholate; Gelucire® 44/14, etc.

In some embodiments, the celecoxib compositions of present application comprises at least one solubilizer selected from the group consisting of, glycerol polyethylene glycol ricinoleate, macrogolglycerol ricinoleate Ph. Eur., polyoxyl 35 castor Oil lauroyl polyoxyl-32 glycerides, lauroyl macrogol-32glycerides, polyoxyl 40 hydrogenated castor oil, Polyoxyl 35 castor oil, PEG-40 Hydrogenated Castor Oil, or mixtures thereof.

The at least one solubilizer may be present in the stable oral liquid pharmaceutical compositions disclosed herein in a variety of concentrations. For example, the stable oral liquid pharmaceutical compositions disclosed herein can comprise at least one solubilizer of at least 10% by weight, at least 20% by weight, at least 30% by weight, at least 40% by weight, at least 50% by weight, at least 60% by weight, at least 70% by weight, at least 80% by weight, at least 90% by weight, or a percentage between any two of the above values, based on the total weight of the composition. In some embodiments, the celecoxib composition of present application comprises of at least one solubilizer in an amount of from about 10% to about 70% by weight, or from about 20% to about 60% by weight, or from about 20% to about 50% by weight, or from about 30% to about 40% by weight, based on the total weight of the composition.

In certain aspects of the above embodiments, the celecoxib composition of present application comprises solubilizer and polar solvent in a weight ratio of from about 0.60:1.00 to about 1.8:1.00.

In another aspect of above embodiments, the present application provides a stable liquid oral pharmaceutical composition of celecoxib comprising therapeutically effective amount of celecoxib, at least one solubilizer and at least one polar solvent, wherein said composition comprises solubilizer and polar solvent in weight ratio of from about 0.60:1.00 to about 1.8:1.00.

In certain aspects of the above embodiments, the present application provides a stable oral liquid pharmaceutical composition of celecoxib comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in weight ratio of from about 0.60:1.00 to about 1.8:1.00.

In an aspect of the above embodiments, the compositions of the present application comprises celecoxib in an amount of from about 1% to about 80% by weight, or from about 2% to about 70% by weight, or from about 2% to about 50% by weight, or from about 2% to about 40% by weight, or from about 2% to about 8% by weight, based on the total weight of the composition.

In some embodiments, the present application provides a stable oral liquid pharmaceutical composition of celecoxib comprising, therapeutically effective amount of celecoxib, at least one solubilizer and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and celecoxib in weight ratio of from about 4.0:1.0 to about 20:1.0.

In some embodiments, the celecoxib compositions of present application comprises of at least one medium chain glyceride and celecoxib in a weight ratio of from about 2.0:1.0 to about 20:1.0. In some embodiments, compositions of present application comprises of at least one medium chain glyceride and celecoxib in a weight ratio of from about 2.0:1.0 to about 10.0:1.0.

In some embodiments, the celecoxib compositions of present application comprises of at least one solubilizer and at least one medium chain glyceride in a weight ratio of from about 0.05:1.0 to about 20:1.0. In some embodiment, celecoxib composition of present application comprises of at least one solubilizer and at least one medium chain glyceride in a ratio of from about 0.05:1.0 to about 10.0:1.0.

In some embodiments, the celecoxib composition of present application comprises of at least one solubilizer and celecoxib in a weight ratio of from about 4.0:1.0 to about 20:1.0.

In some embodiments, the present application provides a pharmaceutical composition of celecoxib comprising:

-   -   a. therapeutically effective amount of celecoxib;     -   b. at least one solubilizer in amount from about 35% w/w to         about 45% w/w;     -   c. at least one polar solvent in amount from about 25% w/w to         about 42% w/w; and     -   d. at least one pharmaceutically acceptable excipient,         wherein said solubilizer and polar solvent are present in the         weight ratio of from about 0.60:1.00 to about 1.8:1.00 and does         not show any precipitation in Fasted-State Simulated Gastric         Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and         under stirring at a speed of 50 rpm at least for 60 minutes.         Improved Pharmacokinetic Parameters

The stable oral liquid pharmaceutical compositions disclosed herein can have a variety of pharmacokinetic parameters. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein can have an improved pharmacokinetic parameter in comparison to a conventional celecoxib oral composition, such as AUC_((0-15min)), AUC_((0-30min)), AUC_((0-1hr)), AUC_((0-2hr)), AUC_((0-t)), AUC_((0-∞)), T_(lag), T_(max), etc.

In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein, upon oral administration to a human subject under fasting conditions provides T_(lag) of not more than 60 minutes, not more than 30 minutes, not more than 20 minutes, not more than 10 minutes, not more than 8 minutes, not more than 6 minutes, not more than 5 minutes, not more than 4 minutes, not more than 3 minutes, not more than 2 minutes, not more than 1 minute, or less. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein, upon oral administration to a human subject under fasting conditions provides T_(max) of less than about 120 minutes, less than about 90 minutes, less than about 80 minutes, less than about 70 minutes, less than about 60 minutes, less than about 50 minutes, less than about 40 minutes, less than about 30 minutes, less than about 20 minutes, or less. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein, upon oral administration to a human subject under fasting conditions provides AUC_((0-15min)) of at least about 1 ng·h/mL, at least about 2 ng·h/mL, at least about 5 ng·h/mL, at least about 10 ng·h/mL, at least about 20 ng·h/mL, at least about 30 ng·h/mL, at least about 40 ng·h/mL, at least about 50 ng·h/mL, at least about 100 ng·h/mL, at least about 200 ng·h/mL, or more, or a range between any two of the above values. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein, upon oral administration to a human subject under fasting conditions provides AUC_((0-30min)) of at least about 10 ng·h/mL, at least about 20 ng·h/mL, at least about 30 ng·h/mL, at least about 40 ng·h/mL, at least about 50 ng·h/mL, at least about 60 ng·h/mL, at least about 70 ng·h/mL, at least about 80 ng·h/mL, at least about 90 ng·h/mL, at least about 100 ng·h/mL, at least about 200 ng·h/mL, at least about 500 ng·h/mL, or more, or a range between any two of the above values. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein, upon oral administration to a human subject under fasting conditions provides AUC_((0-1hr)) of at least about 100 ng·h/mL, at least about 200 ng·h/mL, at least about 300 ng·h/mL, at least about 400 ng·h/mL, at least about 500 ng·h/mL, at least about 600 ng·h/mL, at least about 700 ng·h/mL, at least about 800 ng·h/mL, at least about 900 ng·h/mL, at least about 1000 ng·h/mL, at least about 1500 ng·h/mL, at least about 2000 ng·h/mL, at least about 3000 ng·h/mL, at least about 4000 ng·h/mL, or more, or a range between any two of the above values. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein, upon oral administration to a human subject under fasting conditions provides AUC_((0-2hr)) of at least about 500 ng·h/mL, at least about 600 ng·h/mL, at least about 700 ng·h/mL, at least about 800 ng·h/mL, at least about 900 ng·h/mL, at least about 1000 ng·h/mL, at least about 1500 ng·h/mL, at least about 2000 ng·h/mL, at least about 3000 ng·h/mL, at least about 4000 ng·h/mL, at least about 5000 ng·h/mL, at least about 6000 ng·h/mL, at least about 7000 ng·h/mL, at least about 8000 ng·h/mL, or more, or a range between any two of the above values. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein, upon oral administration to a human subject under fasting conditions provides AUC_((0-t)) of at least about 500 ng·h/mL, at least about 600 ng·h/mL, at least about 700 ng·h/mL, at least about 800 ng·h/mL, at least about 900 ng·h/mL, at least about 1000 ng·h/mL, at least about 1500 ng·h/mL, at least about 2000 ng·h/mL, at least about 3000 ng·h/mL, at least about 4000 ng·h/mL, at least about 5000 ng·h/mL, at least about 6000 ng·h/mL, at least about 7000 ng·h/mL, at least about 8000 ng·h/mL, or more, or a range between any two of the above values. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein, upon oral administration to a human subject under fasting conditions provides AUC_((0-∞)) of at least about 500 ng·h/mL, at least about 600 ng·h/mL, at least about 700 ng·h/mL, at least about 800 ng·h/mL, at least about 900 ng·h/mL, at least about 1000 ng·h/mL, at least about 1500 ng·h/mL, at least about 2000 ng·h/mL, at least about 3000 ng·h/mL, at least about 4000 ng·h/mL, at least about 5000 ng·h/mL, at least about 6000 ng·h/mL, at least about 7000 ng·h/mL, at least about 8000 ng·h/mL, or more, or a range between any two of the above values.

In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein, upon oral administration to a human subject under fasting conditions have a release rate of no less than 50%, no less than 60%, no less than 70%, no less than 80%, no less than 90%, at a period of 10 minutes. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein, upon oral administration to a human subject under fasting conditions have a release rate of no less than 50%, no less than 60%, no less than 70%, no less than 80%, no less than 90%, at a period of 15 minutes. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein have a release rate of no less than 50%, no less than 60%, no less than 70%, no less than 80%, no less than 90%, at a period of 10 minutes in 900 ml of 0.01N HCl with 0.5% sodium lauryl sulphate (SLS), when tested in a USP Type 2 apparatus with sinkers at 50 rpm and 37° C. In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein have a release rate of no less than 50%, no less than 60%, no less than 70%, no less than 80%, no less than 90%, at a period of 15 minutes in 900 ml of 0.01N HCl with 0.5% sodium lauryl sulphate (SLS), when tested in a USP Type 2 apparatus with sinkers at 50 rpm and 37° C.

In some embodiments, the celecoxib compositions of present application comprises reduced dose of celecoxib, wherein said composition provides similar or higher AUC_((0-15min)), AUC_((0-30 min)), AUC_((0-1hour)), and AUC_((0-2hour)′) compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises reduced dose of celecoxib, wherein said composition provides AUC_((0-15min)) of at least 50 times higher compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises reduced dose of celecoxib, wherein said composition provides AUC_((0-30min)) of at least 12 times higher compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises reduced dose of celecoxib, wherein said composition provides AUC_((0-1hour)) of at least 5 times higher compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises reduced dose of celecoxib, wherein said composition provides AUC_((0-2hour)) of at least 1.5 times higher compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises reduced dose of celecoxib, wherein said composition provides similar or higher AUC_((0-15min)), AUC_((0-30min)), AUC_((0-1hour)), and AUC_((0-2hour)′) compared to conventional celecoxib compositions comprising 400 mg of celecoxib such as CELEBREX® 400 mg oral capsules.

In some embodiments, the present application provides an oral liquid pharmaceutical composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application provides an oral liquid pharmaceutical composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00 and upon oral administration to a human subject under fasting conditions provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride and at least one pharmaceutically acceptable excipient; wherein said composition

-   -   a) releases no less than 70% at a period of 10 minutes; or     -   b) releases no less than 80% at a period of 15 minutes,         in 900 ml of 0.01N HCl with 0.5% sodium lauryl sulphate (SLS),         when tested in a USP Type 2 apparatus with sinkers at 50 rpm and         37° C.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient; wherein said composition

-   -   a) releases no less than 70% at a period of 10 minutes; or     -   b) releases no less than 80% at a period of 15 minutes, in 900         ml of 0.01N HCl with 0.5% sodium lauryl sulphate (SLS), when         tested in a USP Type 2 apparatus with sinkers at 50 rpm and 37°         C.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-15min)) at least about 10 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-30min)) at least about 80 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-1hr)) at least about 400 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-2hr)) at least about 1000 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-t)) of at least about 2000 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-∞)) of at least about 2000 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides T_(lag) of not more than 10 minutes.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides T_(lag) of not more than 8 minutes.

In some embodiments, the celecoxib composition of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides T_(lag) of not more than 5 minutes.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides T_(max) of less than about 90 minutes.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides T_(max) of less than about 60 minutes.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-15min)) at least about 10 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL.

In some embodiments, the celecoxib compositions of the present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-30min)) at least about 80 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-1hr)) at least about 400 ng·h/mL.

In some embodiments the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-2hr)) at least about 1000 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00 and; said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00 and upon oral administration to a human subject under fasting conditions provides AUC_((0-t)) of at least about 2000 ng·h/mL.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-∞)) of at least about 2000 ng·h/mL

In some embodiments, the compositions of celecoxib of the present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides T_(lag) of not more than 10 minutes.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides T_(lag) of not more than 8 minutes.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides T_(lag) of not more than 5 minutes.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the weight ratio of from about 0.60:1.00 to about 1.8:1.00; and said composition upon oral administration to a human subject under fasting conditions provides T_(max) of less than about 90 minutes.

Improved Physical Properties

In some embodiments, the stable oral liquid pharmaceutical compositions disclosed herein possess improved physical properties, such as droplet size, viscosity, etc. The D50 and D90 represent, the median or the 50^(th) percentile and the 90^(th) percentile of the oil droplet size distribution, respectively, as measured by volume. This means, the term “D50” is defined as the size in nm (nanometers) below which 50 percent of the oil droplets reside on a volume basis and similarly, the term “D90” is defined as the size in nm (nanometers) below which 90% of the oil droplets reside, on a volume basis. Oil droplet size can be determined, for example, by laser light scattering using a particle size analyzer, such as the proprietary Zetasizer™ apparatus available from Malvern Instruments Ltd.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride and at least one pharmaceutically acceptable excipient, wherein said compositions does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes and said composition has a mean oil droplet size of not more than 500 nm.

A ternary phase diagram is drawn (FIG. 1) which depicts the “stable composition region A”. The “stable composition region A” is defined by shaded region or the region between the connecting lines between six points (a, b, c, d, e and f). Any composition that is outside of this region does not form an acceptable composition because either the onset of precipitation time is less than 60 minutes; D50 oil droplet size is more than about 250 nm or D90 oil droplet size is more than about 500 nm.

In one embodiment, stable compositions of celecoxib as per present application that comprises

-   -   a) therapeutically effective amount of celecoxib, at least one         solubilizer, at least one medium chain glyceride; and     -   b) polar solvent comprising mixture of ethanol and glycerin;     -   wherein the composition falls within the shaded region of a         phase diagram, as shown in FIG. 1, wherein boundaries of a         stable composition are defined by shaded region or the region         between the connecting lines between the six points (a, b, c, d,         e and f), wherein the composition comprises about 1% to about         80% w/w celecoxib and correspond to a weight % ratio of base         composition:ethanol:glycerin of 0.200:0.024:0.712 for a,         0.200:0.376:0.360 for b, 0.200:0.400:0.336 for c,         0.536:0.400:0.000 for d, 0.900:0.036:0.00 for e and         0.900:0.00:0.036 for f.

A ternary phase diagram is drawn FIG. 2 which depicts the “stable composition region B”. The “stable composition region B” is defined by shaded region or the region between the connecting lines between six points (a, b, c, d, e and f). Any composition that is outside of this region does not form an acceptable composition because either the onset of precipitation time is less than 60 minutes; D50 oil droplet size is more than about 125 nm or D90 oil droplet size is more than about 250 nm.

In one embodiment, stable compositions of celecoxib as per present application that comprises

-   -   a) therapeutically effective amount of celecoxib, at least one         solubilizer, at least one medium chain glyceride; and     -   b) polar solvent comprising mixture of ethanol and glycerin;     -   wherein the composition falls within shaded region of a phase         diagram, as shown in FIG. 2, wherein boundaries of a stable         composition are defined by shaded region or the region between         the connecting lines between the six points (a, b, c, d, e and         f), wherein the composition comprises about 1% to about 80% w/w         celecoxib and correspond to a weight % ratio of base         composition:ethanol:glycerin of 0.226:0.000:0.710 for a,         0.235:0.371:0.330 for b, 0.236:0.400:0.300 for c,         0.536:0.400:0.000 for d, 0.865:0.071:0.000 for e and         0.836:0.000:0.100 for f.

A ternary phase diagram is drawn (FIG. 3) which depicts the “stable composition region C”. The “stable composition region C” is defined by shaded region or the region between the connecting lines between eight points (a, b, c, d, e, f, g and h). Any composition that is outside of this shaded region does not form an acceptable composition because either the onset of precipitation time is less than 60 minutes; D50 oil droplet size is more than about 50 nm or D90 oil droplet size is more than about 100 nm.

In one embodiment, stable compositions of celecoxib as per present application that comprises

-   -   c) therapeutically effective amount of celecoxib, at least one         solubilizer, at least one medium chain glyceride; and     -   d) polar solvent comprising mixture of ethanol and glycerin;     -   wherein the composition falls within region of a phase diagram,         as shown in FIG. 3, wherein boundaries of a stable composition         are defined by shaded region or the region between the         connecting lines between the eight points (a, b, c, d, e, f, g         and h) wherein the composition comprises about 1% to about 80%         w/w celecoxib and correspond to a weight % ratio of base         composition:ethanol:glycerin is 0.300:0.000:0.636 for a,         0.385:0.206:0.345 for b, 0.283:0.399:0.254 for c,         0.536:0.400:0.000 for d, 0.745:0.191: 0.000 for e, 0.778:0.144:         0.014 for f, 0.817:0.056:0.063 for g and 0.636:0.000:0.300 for         h.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” within the region of the phase diagrams, wherein the compositions comprises reduced dose of celecoxib, wherein the reduced dose of celecoxib provides similar or higher AUC_((0-15min)), AUC_((0-30min)), AUC_((0-1hour)), and AUC_((0-2hour)) compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In another aspect of above embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of the phase diagrams, wherein the compositions are essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In another aspect of above embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of the phase diagrams, wherein the compositions

-   -   a) releases no less than 70% at a period of 10 minutes; or     -   b) releases no less than 80% at a period of 15 minutes,         in 900 ml of 0.01N HCl with 0.5% sodium lauryl sulphate (SLS),         when tested in a USP Type 2 apparatus with sinkers at 50 rpm and         37° C.

In another aspect of above embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of the phase diagrams, wherein said composition in the form of a solution, suspension, emulsion or liquid mixture.

In another aspect of above embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of the phase diagrams, wherein said composition has a viscosity of from about 20 cps to about 1000 cps and has a density of from about 0.8 gm/cm³ to about 2 gm/cm³.

In another aspect of above embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of the phase diagrams, wherein the composition has transmittance of at least 40%.

In another aspect of above embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of the phase diagrams, wherein the composition has pH of from about 3 to about 7.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of the phase diagrams, wherein said composition

-   -   c) releases no less than 70% at a period of 10 minutes; or     -   a) releases no less than 80% at a period of 15 minutes,         in 900 ml of 0.01N HCl with 0.5% sodium lauryl sulphate (SLS),         when tested in a USP Type 2 apparatus with sinkers at 50 rpm and         37° C.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of a phase diagrams, wherein the composition upon oral administration to a human subject under fasting conditions provides AUC_((0-15min)) at least about 10 ng·h/mL.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B”, and “stable composition region C” shown in the shaded region of a phase diagram, wherein the composition upon oral administration to a human subject under fasting conditions provides AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of the phase diagram, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-30min)) at least about 80 ng·h/mL.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of the phase diagrams, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of the phase diagrams, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-1hr)) at least about 400 ng·h/mL.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of a phase diagrams, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of a phase diagrams, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-2hr)) at least about 1000 ng·h/mL.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of a phase diagrams, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of a phase diagrams, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-t)) of at least about 2000 ng·h/mL.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of a phase diagrams, wherein said composition upon oral administration to a human subject under fasting conditions provides AUC_((0-∞)) of at least about 2000 ng·h/mL.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of a phase diagrams, wherein said composition upon oral administration to a human subject under fasting conditions provides T_(lag) of not more than 8 minutes.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B” and “stable composition region C” shown in the shaded region of a phase diagrams, wherein said composition upon oral administration to a human subject under fasting conditions provides Tmax of less than about 90 minutes.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B”, and “stable composition region C” shown in the shaded region of a phase diagrams, wherein said composition upon oral administration to a human subject under fasting conditions provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the stable compositions depicted by “stable composition region A”, “stable composition region B”, and “stable composition region C” shown in the shaded region of a phase diagrams, wherein said composition comprising reduced dose of celecoxib upon oral administration to a human subject under fasting conditions provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

The stable oral liquid pharmaceutical compositions disclosed herein can comprise a variety of mean oil droplet sizes. In some embodiments, the composition provides mean oil droplet size of not more than 500 nm, not more than 250 nm, not more than 100 nm, not more than 50 nm.

In some embodiments, the celecoxib composition of present application is stable and does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes and said composition has a mean oil droplet size of not more than 500 nm.

In some embodiments, the celecoxib composition of present application is stable and does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes and said composition has a mean oil droplet size of not more than 250 nm.

In some embodiments, the celecoxib composition of present application is stable and does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes and said composition has a mean oil droplet size of not more than 100 nm.

In some embodiments, the celecoxib composition of present application is stable and does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes and said composition has a mean oil droplet size of composition is not more than 50 nm.

The stable oral liquid pharmaceutical compositions disclosed herein can comprise a variety of viscosities. In some embodiments, the stable oral liquid composition of celecoxib of the present application has a viscosity that is about 20 cps, about 40 cps, about 60 cps, about 80 cps, about 100 cps, about 200 cps, about 500 cps, about 1000 cps, or a range between any two of the above values.

The stable oral liquid pharmaceutical compositions disclosed herein can comprise a variety of densities. In some embodiments, the stable oral liquid composition of celecoxib of the present application has a density of from about 0.8 gm/cm³ to about 2 gm/cm³′

In some embodiment, the composition provides mean oil droplet size of not more than 500 nm or not more than 250 nm or not more than 100 nm or not more than 50 nm.

In some embodiments, the stable oral liquid composition of the present application has a viscosity of from about 20 cps to about 1000 cps.

In some embodiments, the stable oral liquid composition of the present application has a density of from about 0.8 gm/cm³ to about 2 gm/cm³′

In some embodiments, the stable oral liquid composition of the present application has transmittance of at least 40%.

In some embodiments, the stable oral liquid composition of the present application has a pH of from about 3 to about 7.

In some embodiments, the celecoxib compositions of present application further comprises of water in amount less than about 10%, based on total weight of the composition.

The stable oral liquid pharmaceutical compositions disclosed herein can comprise a variety of transmittances. In some embodiments, the stable oral liquid composition of celecoxib of present application has transmittance of at least 40%. In some embodiments, the stable oral liquid composition of celecoxib of present application has transmittance of more than 40%.

The stable oral liquid pharmaceutical compositions disclosed herein can comprise a variety of pH values. In some embodiments, the stable oral liquid composition of celecoxib of present application has pH of from about 3 to about 7.

In some embodiments, the present application provides a stable oral liquid pharmaceutical composition of celecoxib comprising:

-   -   a. therapeutically effective amount of celecoxib;     -   b. at least one solubilizer in amount from about 35% w/w to         about 45% w/w;     -   c. at least one polar solvent in amount from about 25% w/w to         about 42% w/w; and     -   d. at least one pharmaceutically acceptable excipient,         wherein said solubilizer and polar solvent are present in the         weight ratio of from about 0.60:1.00 to about 1.8:1.00 and         wherein said composition has a viscosity of from about 20 cps to         about 1000 cps and density of from about 0.8 gm/cm³ to about 2         gm/cm³.         Improved Stability

In some embodiments, present application relates to a composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride and at least one pharmaceutically acceptable excipient, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes.

In some embodiments, the stable oral liquid composition of celecoxib of the present application is essentially free of precipitation inhibitors such as polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In some embodiments, the present application provides a stable oral pharmaceutical composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride and at least one pharmaceutically acceptable excipient, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 30 min or 60 min or 90 min or 120 minutes or 180 minutes or 240 minutes time points; and said composition is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In some embodiments, the present application provides a stable oral liquid pharmaceutical composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride and at least one pharmaceutically acceptable excipients, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 30 min or 60 min or 90 min or 120 minutes or 180 minutes or 240 minutes time points; and said composition is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In some embodiment, the composition provides mean oil droplet size of not more than 500 nm or not more than 250 nm or not more than 100 nm or not more than 50 nm.

In some embodiments, the stable oral liquid composition of the present application has a viscosity of from about 20 cps to about 1000 cps.

In some embodiments, the stable oral liquid composition of the present application has a density of from about 0.8 gm/cm³ to about 2 gm/cm'^(.)

In some embodiments, the stable oral liquid composition of the present application has transmittance of at least 40%.

In some embodiments, the stable oral liquid composition of the present application has a pH of from about 3 to about 7.

In some embodiments, the present application provides a stable oral liquid pharmaceutical composition of celecoxib comprising:

-   -   a. therapeutically effective amount of celecoxib;     -   b. at least one solubilizer in amount from about 35% w/w to         about 45% w/w;     -   c. at least one polar solvent in amount from about 25% w/w to         about 42% w/w; and     -   d. at least one pharmaceutically acceptable excipient,         wherein said solubilizer and polar solvent are present in the         weight ratio of from about 0.60:1.00 to about 1.8:1.00 and shows         no precipitation in Fasted-State Simulated Gastric Fluid         (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under         stirring at a speed of 50 rpm at least for 60 minutes.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer and at least one medium chain glyceride, wherein said composition shows no precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes.

In some embodiments, present application relates to a composition comprising therapeutically effective amount of celecoxib, at least one solubilizer and at least one pharmaceutically acceptable excipient, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes.

In some embodiments, the present application provides a stable oral pharmaceutical composition comprising therapeutically effective amount of celecoxib, at least one solubilizer and at least one pharmaceutically acceptable excipient, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 30 min or 60 min or 90 min or 120 minutes or 180 minutes or 240 minutes time points; and said composition is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In some embodiments, the present application provides a stable oral liquid pharmaceutical composition comprising therapeutically effective amount of celecoxib, at least one solubilizer and at least one pharmaceutically acceptable excipient, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 30 min or 60 min or 90 min or 120 minutes or 180 minutes or 240 minutes time points; and said composition is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In some embodiments, the present application provides a pharmaceutical composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes.

In some embodiments, the present application provides a stable oral pharmaceutical composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 30 min or 60 min or 90 min or 120 minutes or 180 minutes or 240 minutes time points; and said composition is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In some embodiments, the present application provides a stable oral liquid pharmaceutical composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipients, wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, when measured at 30 min or 60 min or 90 min or 120 minutes or 180 minutes or 240 minutes time points; and said composition is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In some embodiments, the oral liquid composition of present application has a viscosity of from about 20 cps to about 1000 cps.

In some embodiments, the oral liquid composition of present application has a density of from about 0.8 gm/cm³ to about 2 gm/cm³.

In some embodiments, the celecoxib composition of present application do not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 240 minutes.

In some embodiments, the celecoxib composition of present application is essentially free of precipitation inhibitors such as polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose, and hydroxypropyl methylcellulose.

In some embodiments, the present application provides a composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient; wherein said composition provides mean oil droplet size of no more than 500 nm, when subjected to Fasted-State Simulated Gastric Fluid (FaSSGF) at pH of 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm, measured at 30 min or 60 min or 90 min or 120 minutes or 180 minutes or 240 minutes time points.

In some embodiments, the celecoxib compositions of present application comprises of therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, and wherein said composition does not show any precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 240 minutes.

Reduced Dose

It is observed that the oral liquid celecoxib composition of present application exhibits increased bioavailability (AUC_((0-15min)), AUC_((0-30min)), AUC_((0-1hour)), AUC_((0-2hour)) and require smaller dose as compared to conventional composition of celecoxib such as CELEBREX® oral capsules. Thus, oral compositions with lower dose or reduced dose of celecoxib that can achieve the same or better therapeutic effects as observed with larger doses of conventional celecoxib compositions are desired to minimize the adverse effects of celecoxib.

In some embodiments, the compositions of celecoxib of the present application comprises reduced dose of celecoxib, wherein reduced dose of celecoxib provides the same or better therapeutic effects compared to conventional composition of celecoxib such as CELEBREX® oral capsules.

In some embodiments, the compositions of celecoxib of the present application comprises reduced dose of celecoxib, wherein reduced dose of celecoxib provides similar or higher AUC_((0-15min)), AUC_((0-30min)), AUC_((0-1hour)), and AUC_((0-2hour)) compared to conventional composition of celecoxib such as CELEBREX® oral.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein the reduction in dose of celecoxib is at least 20% compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein the reduction in dose of celecoxib is at least 30% compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein the reduction in dose of celecoxib is at least 40% compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein the reduction in dose of celecoxib is at least 50% compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein the reduction in dose of celecoxib is at least 60% compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein the reduction in dose of celecoxib is at least 70% compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein the reduction in dose of celecoxib is at least 80% compared to conventional celecoxib compositions such as CELEBREX® oral capsules.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein the reduction in dose of celecoxib is at least 40% compared to conventional celecoxib compositions comprising 400 mg of celecoxib such as CELEBREX® 400 mg oral capsules.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein the reduction in dose of celecoxib is at least 55% compared to conventional celecoxib compositions comprising 400 mg of celecoxib such as CELEBREX® 400 mg oral capsules.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein the reduction in dose of celecoxib is at least 70% compared to conventional celecoxib compositions comprising 400 mg of celecoxib such as CELEBREX® 400 mg oral capsules.

In some embodiments, the celecoxib compositions of present application comprises reduced dose of celecoxib, wherein said reduced dose is from about 100 mg to 250 mg of celecoxib.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein said reduced dose is about 240 mg.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein said reduced dose is about 180 mg.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein said reduced dose is about 120 mg.

In some embodiments, the celecoxib compositions of present application comprises of reduced dose of celecoxib, wherein the reduction in dose of celecoxib is at least 70% compared to conventional celecoxib compositions comprising 400 mg of celecoxib such as CELEBREX® 400 mg oral capsules.

In some embodiments, the celecoxib compositions of present application comprises reduced dose of celecoxib, wherein said reduced dose is from about 100 mg to 250 mg of celecoxib.

In some embodiments, the stable oral liquid celecoxib composition of present application is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose, and hydroxypropyl methylcellulose.

In some embodiments, the present application provides an oral liquid pharmaceutical composition comprises reduced dose of celecoxib, where in the said reduced dose comprises of from about 100 mg to 250 mg of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition upon oral administration to a human subject under fasting conditions provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application provides an oral liquid pharmaceutical composition comprise reduced dose of celecoxib, where in the said reduced dose comprises of from about 100 mg to 250 mg of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the ratio of from about 0.60:1.00 to about 1.8:1.00 and upon oral administration to a human subject under fasting conditions provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application provides an oral liquid pharmaceutical composition of celecoxib, wherein said composition comprises of from about 100 mg to 250 mg of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises solubilizer and polar solvent in the ratio of from about 0.60:1.00 to about 1.8:1.00 and upon oral administration to a human subject under fasting conditions provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.         Pharmaceutically Acceptable Excipients, Flavoring and Sweetening         Agents

In some embodiments, the celecoxib compositions of present application may further contain at least one flavoring agent or taste masking agent. These flavoring agents or taste masking agents are well known in art or approved by US FDA.

Non-limiting exemplary list of flavoring agents/taste masking agents: natural and synthetic flavoring liquids such as volatile oils, synthetic flavor oils, flavoring aromatic oils, liquids, oleoresins or extracts derived from plants, leaves, flowers, fruits, stems and combinations thereof. Non-limiting representative examples of volatile oils include spearmint oil, cinnamon oil, oil of wintergreen (methyl salicylate), peppermint oil, menthol, clove oil, bay oil, anise oil, eucalyptus oil, thyme oil, cedar leaf oil, oil of nutmeg, allspice oil, oil of sage, mace extract, oil of bitter almond, and cassia oil. Also artificial, natural or synthetic flavors including fruit flavors such as vanilla, and citrus oils including lemon, orange, grape, lime and grapefruit and fruit essences including apple, pear, peach, grape, strawberry, raspberry, cherry, plum, pineapple, apricot, banana and other useful flavorings include aldehydes and esters such as benzaldehyde (cherry, almond), citral, i.e., alphocitral (lemon, lime), neral, i.e., beta-citral (lemon, lime), decanal (orange, lemon), aldehyde C-8 (citrus fruits), aldehyde C-9 (citrus fruits), aldehyde C-12 (citrus fruits), tolyl aldehyde (cherry, almond), 2,6-dimethyloctanal (green fruit), and 2-dodecenal (citrus, mandarin), bubble gum flavor, mixtures thereof and the like.

Non-limiting exemplary list of sweeteners: sugars such as sucrose, glucose (corn syrup), dextrose, invert sugar, fructose, and mixtures thereof, saccharin and its various salts such as the sodium or calcium salt; cyclamic acid and its various salts such as the sodium salt; the dipeptide sweeteners such as aspartame, acesulfame K, and other sweeteners like magnasweet, sucralose, mixtures thereof and the like.

Methods of Treating Pain

In some embodiments, the present application relates to a method of treating pain in a human subject by orally administering a stable oral liquid pharmaceutical composition as disclosed herein. In some embodiments, the composition comprises a therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride and at least one pharmaceutically acceptable excipient, wherein said composition shows no precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes.

In some embodiments, the present application relates to a method of treating pain in a human subject by orally administering a composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one polar solvent, at least one medium chain glyceride and at least one pharmaceutically acceptable excipient, wherein said composition shows no precipitation in Fasted-State Simulated Gastric Fluid (FaSSGF) at pH 2.0, temperature of 37° C.±0.5° C. and under stirring at a speed of 50 rpm at least for 60 minutes.

In some embodiment, the composition provides mean oil droplet size of no more than 1000 nm or not more than 500 nm or not more than 250 nm or not more than 100 nm or not more than 50 nm.

In some embodiments, the present application relates to a method for treating pain in a human subject by orally administering a composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition comprises of said solubilizer and polar solvent in the ratio of from about 0.60:1.00 to about 1.8:1.00.

In some embodiments, the present application relates to a method for treating pain in a human subject by orally administering a composition comprising therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, at least one polar solvent and at least one pharmaceutically acceptable excipient, wherein said composition is essentially free of precipitation inhibitors such as, polyoxyethylene-polyoxypropylene block copolymers, pluronics, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropyl methylcellulose.

In some embodiments, the present application relates to a method for treating pain in a human subject by orally administering a composition comprising therapeutically effective amount of celecoxib, wherein the composition has transmittance of at least 40%.

In some embodiments, the present application relates to a method for treating pain in a human subject by orally administering a composition comprising therapeutically effective amount of celecoxib, wherein the composition has pH of from about 3 to about 7.

In some embodiments, the present application relates to a method for treating pain in a human subject by administering an oral liquid pharmaceutical composition of celecoxib comprising:

-   -   a) therapeutically effective amount of celecoxib;     -   b) at least one solubilizer in an amount from about 35% w/w to         about 45% w/w; and     -   c) at least one polar solvent in an amount from about 25% w/w to         about 42% w/w;     -   d) at least one pharmaceutically acceptable excipients;         wherein said solubilizer and polar solvent are present in the         ratio of from about 0.60:1.00 to about 1.8:1.00 and wherein said         composition has a viscosity of from about 20 cps to about 1000         cps and density of from about 0.8 gm/cm³ to about 2 gm/cm³.

In some embodiments, the present application relates to a method for treating pain in a human subject by administering an oral liquid pharmaceutical composition of celecoxib comprising:

-   -   a) reduced dose of celecoxib, wherein the reduction in dose of         celecoxib is at least 20 percent compared to conventional         celecoxib compositions;     -   b) at least one solubilizer in an amount from about 35% w/w to         about 45% w/w; and     -   c) at least one polar solvent in an amount from about 25% w/w to         about 42% w/w;     -   d) at least one pharmaceutically acceptable excipients;         wherein said solubilizer and polar solvent are present in the         weight ratio of from about 0.60:1.00 to about 1.8:1.00 and         wherein said composition has a viscosity of from about 20 cps to         about 1000 cps and density of from about 0.8 gm/cm³ to about 2         gm/cm³.

In some embodiments, the present application relates to a method for treating pain in a human subject by administering an oral liquid pharmaceutical composition of celecoxib, wherein said composition provides at least one of the following pharmacokinetic parameters upon oral administration to a human subject under fasting conditions:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for providing pain freedom in a human subject suffering from pain by administering an oral pharmaceutical composition of celecoxib, wherein said composition provides at least one of the following pharmacokinetic parameters upon oral administration to a human subject under fasting conditions:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for providing pain freedom in a human subject suffering from pain, said method comprising administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib and at least one pharmaceutically acceptable excipient, whereby the subject is provided with pain freedom at 2 hours following administration, wherein said composition upon oral administration to a human subject under fasting conditions, provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15 min)) from about 10 ngh/mL to about 80 ngh/mL;     -   b) AUC_((0-30 min)) from about 80 ngh/mL to about 400 ngh/mL;     -   c) AUC_((0-1hr)) from about 400 ngh/mL to about 1500 ngh/mL;     -   d) AUC_((0-2hr)) from about 1000 ngh/mL to about 4000 ngh/mL;     -   e) AUC_((0-t)) at least about 2000 ngh/mL;     -   f) AUC_((0-∞)) of at least about 2000 ngh/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for providing partial pain relief in a human subject suffering from a pain, said method comprising administering to the subject a stable oral pharmaceutical composition comprising atherapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, whereby the subject is provided with pain relief in less than about 2 hours following administration, wherein said composition upon oral administration to a human subject under fasting conditions provides at least one of the following pharmacokinetic parameters:

-   -   h) AUC_((0-15 min)) from about 10 ngh/mL to about 80 ngh/mL;     -   i) AUC_((0-30 min)) from about 80 ngh/mL to about 400 ngh/mL;     -   j) AUC_((0-1hr)) from about 400 ngh/mL to about 1500 ngh/mL;     -   k) AUC_((0-2hr)) from about 1000 ngh/mL to about 4000 ngh/mL;     -   l) AUC_((0-t)) at least about 2000 ngh/mL;     -   m) AUC_((0-∞)) of at least about 2000 ngh/mL; and     -   n) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for providing partial pain relief in less than about 2 hours in a human subject suffering from a pain by administering an oral pharmaceutical composition of celecoxib, wherein said composition provides at least one of the following pharmacokinetic parameters upon oral administration to a human subject under fasting conditions:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for reducing the most bothersome symptoms in a human subject suffering from migraine by administering an oral pharmaceutical composition of celecoxib, wherein said composition provides at least one of the following pharmacokinetic parameters upon oral administration to a human subject under fasting conditions:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for reducing most bothersome symptoms in a human subject suffering from migraine, said method comprising administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib and at least one pharmaceutically acceptable excipient, whereby the subject is provided with a reduction in the most bothersome symptoms, wherein said composition upon oral administration to a human subject under fasting conditions provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15 min)) from about 10 ngh/mL to about 80 ngh/mL;     -   b) AUC_((0-30 min)) from about 80 ngh/mL to about 400 ngh/mL;     -   c) AUC_((0-1hr)) from about 400 ngh/mL to about 1500 ngh/mL;     -   d) AUC_((0-2hr)) from about 1000 ngh/mL to about 4000 ngh/mL;     -   e) AUC_((0-t)) at least about 2000 ngh/mL;     -   f) AUC_((0-∞)) of at least about 2000 ngh/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for providing pain freedom in a human subject suffering from pain by administering an oral liquid pharmaceutical composition of celecoxib, wherein said composition provides at least one of the following pharmacokinetic parameters upon oral administration to a human subject under fasting conditions:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for providing pain freedom in a human subject suffering from pain, said method comprising administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib and at least one pharmaceutically acceptable excipient, whereby the subject is provided with pain freedom at 2 hours following administration, wherein said composition upon oral administration to a human subject under fasting conditions, provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15 min)) from about 10 ngh/mL to about 80 ngh/mL;     -   b) AUC_((0-30 min)) from about 80 ngh/mL to about 400 ngh/mL;     -   c) AUC_((0-1hr)) from about 400 ngh/mL to about 1500 ngh/mL;     -   d) AUC_((0-2hr)) from about 1000 ngh/mL to about 4000 ngh/mL;     -   e) AUC_((0-t)) at least about 2000 ngh/mL;     -   f) AUC_((0-∞)) of at least about 2000 ngh/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for providing partial pain relief in less than about 2 hours in a human subject suffering from a pain by administering an oral liquid pharmaceutical composition of celecoxib, wherein said composition provides at least one of the following pharmacokinetic parameters upon oral administration to a human subject under fasting conditions:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for providing partial pain relief-in a human subject suffering from a pain, said method comprising administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib, at least one solubilizer, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, whereby the subject is provided with pain relief in less than about 2 hours following administration, wherein said composition upon oral administration to a human subject under fasting conditions provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15 min)) from about 10 ngh/mL to about 80 ngh/mL;     -   b) AUC_((0-30 min)) from about 80 ngh/mL to about 400 ngh/mL;     -   c) AUC_((0-1hr)) from about 400 ngh/mL to about 1500 ngh/mL;     -   d) AUC_((0-2hr)) from about 1000 ngh/mL to about 4000 ngh/mL;     -   e) AUC_((0-t)) at least about 2000 ngh/mL;     -   f) AUC_((0-∞)) of at least about 2000 ngh/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for reducing the most bothersome symptoms in a human subject suffering from migraine by administering an oral liquid pharmaceutical composition of celecoxib, wherein said composition provides at least one of the following pharmacokinetic parameters upon oral administration to a human subject under fasting conditions:

-   -   a) AUC_((0-15min)) from about 10 ng·h/mL to about 80 ng·h/mL;     -   b) AUC_((0-30min)) from about 80 ng·h/mL to about 400 ng·h/mL;     -   c) AUC_((0-1hr)) from about 400 ng·h/mL to about 1500 ng·h/mL;     -   d) AUC_((0-2hr)) from about 1000 ng·h/mL to about 4000 ng·h/mL;     -   e) AUC_((0-t)) of at least about 2000 ng·h/mL;     -   f) AUC_((0-∞)) of at least about 2000 ng·h/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for reducing most bothersome symptoms in a human subject suffering from migraine, said method comprising administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib and at least one pharmaceutically acceptable excipient, whereby the subject is provided with a reduction in the most bothersome symptoms, wherein said composition upon oral administration to a human subject under fasting conditions provides at least one of the following pharmacokinetic parameters:

-   -   a) AUC_((0-15min)) from about 10 ngh/mL to about 80 ngh/mL;     -   b) AUC_((0-30min)) from about 80 ngh/mL to about 400 ngh/mL;     -   c) AUC_((0-1hr)) from about 400 ngh/mL to about 1500 ngh/mL;     -   d) AUC_((0-2hr)) from about 1000 ngh/mL to about 4000 ngh/mL;     -   e) AUC_((0-t)) at least about 2000 ngh/mL;     -   f) AUC_((0-∞)) of at least about 2000 ngh/mL; and     -   g) T_(lag) of not more than 8 minutes.

In some embodiments, the present application relates to a method for treating pain in a human subject by orally administering a composition comprising therapeutically effective amount of celecoxib, wherein the composition has transmittance of at least 40%.

In some embodiments, the present application relates to a method for treating pain in a human subject by orally administering a composition comprising therapeutically effective amount of celecoxib, wherein the composition has pH of from about 3 to about 7.

In some embodiments, the composition of present application is used for the treatment or amelioration of pain including, but not limited to, acute pain, migraine pain, cluster headache, neuropathic pain, post-operative pain, chronic lower back pain, herpes neuralgia, phantom limb pain, central pain, dental pain, neuropathic pain, opioid-resistant pain, visceral pain, surgical pain, bone injury pain, arthritis pain, inflammation, osteoarthritis, juvenile rheumatoid arthritis, ankylosing spondylitis, primary dysmenorrhea, pain during labor and delivery, pain resulting from burns, including sunburn, post-partum pain, angina pain, and genitourinary tract-related pain including cystitis, breakthrough pain, any kind of cancer pain, the term shall also refer to nociceptive pain or nociception in patients need thereof

Methods of Treating Migraine Pain

In some embodiments, the present application relates to a method for providing pain freedom in a human subject suffering from pain, said method comprising administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib and at least one pharmaceutically acceptable excipient, whereby the subject is provided with pain freedom at 2 hours following administration. In some embodiments, the present application relates to a method of treating migraine pain in a human subject by orally administering a stable oral liquid pharmaceutical composition as disclosed herein In some embodiments disclosed herein the methods for providing pain freedom in a human subject suffering from pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib. In some embodiments disclosed herein the methods for providing pain freedom in a human subject suffering from pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib. In some embodiments disclosed herein the methods for providing pain freedom at 2 hours in a human subject suffering from pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib. In some embodiments disclosed herein the methods for providing pain freedom at 2 hours in a human subject suffering from pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib.

In some embodiments, the present application relates to a method for providing partial pain relief-in a human subject suffering from a pain, said method comprising administering to the subject a stable oral pharmaceutical composition comprising of therapeutically effective amount of celecoxib, and at least one pharmaceutically acceptable excipient, whereby the subject is provided with pain relief in less than about 2 hours following administration. In some embodiments, the method for providing partial pain relief in less than about 2 hours in a human subject suffering from a pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib. In some embodiments, the method for providing partial pain relief in less than about 2 hours in a human subject suffering from a pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib. In some embodiments, the methods lead to pain free at 2 hours in at least 25%, at least 26%, at least 27%, at least 28%, at least 29%, at least 30%, at least 31%, at least 32%, at least 33%, at least 34%, at least 35%, or more, of the treated human subjects. In some embodiments, the methods lead to an increase in the percentage of treated human subjects being pain free at 2 hours that is at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or more, in comparison to the percentage of human subjects being treated with a placebo. In some embodiments, the methods lead to partial pain relief at 2 hours in at least 45%, at least 50%, at least 60%, at least 65%, at least 66%, at least 67%, at least 68%, at least 69%, at least 70%, at least 71%, at least 72%, at least 73%, at least 74%, at least 75%, or more, of the treated human subjects. In some embodiments, the methods lead to an increase in the percentage of treated human subjects being partially relieved of pain at 2 hours that is at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, or more, in comparison to the percentage of human subjects being treated with a placebo.

In some embodiments, the present application relates to a method of treating migraine pain in a human subject by orally administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib. In some embodiments, the methods lead to pain free at 2 hours in at least 25%, at least 26%, at least 27%, at least 28%, at least 29%, at least 30%, at least 31%, at least 32%, at least 33%, at least 34%, at least 35%, or more, of the treated human subjects. In some embodiments, the methods lead to an increase in the percentage of treated human subjects being pain free at 2 hours that is at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or more, in comparison to the percentage of human subjects being treated with a placebo. In some embodiments, the methods lead to partial pain relief at 2 hours in at least 45%, at least 50%, at least 60%, at least 65%, at least 66%, at least 67%, at least 68%, at least 69%, at least 70%, at least 71%, at least 72%, at least 73%, at least 74%, at least 75%, or more, of the treated human subjects. In some embodiments, the methods lead to an increase in the percentage of treated human subjects being partially relieved of pain at 2 hours that is at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, or more, in comparison to the percentage of human subjects being treated with a placebo.

In some embodiments, the method for providing partial pain relief in less than about 2 hours in a human subject suffering from a pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said partial pain relief is maintained for at least about 4 hours. In some embodiments, the method for providing partial pain relief in less than about 2 hours in a human subject suffering from a pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said partial pain relief is maintained for at least about 4 hours. In some embodiments, the method for providing partial pain relief in less than about 2 hours in a human subject suffering from a pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said partial pain relief is at least ≥1 level lower pain intensity reported by the human subject suffering from pain, than the predose rating on a numeric rating scale for pain with a range of 0 (no pain) to 3 (severe). In some embodiments, the method for providing partial pain relief in less than about 2 hours in a human subject suffering from a pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said partial pain relief is at least ≥1 level lower pain intensity reported by the human subject suffering from pain, than the predose rating on a numeric rating scale for pain with a range of 0 (no pain) to 3 (severe).

In some embodiments, the present application relates to methods, comprising administering a composition as disclosed herein, lead to pain free at 2 hours in at least 26%, at least 27%, at least 28% or at least 29% or at least 30% of the treated human subjects.

In some embodiments, the present application relates to methods, comprising administering a composition as disclosed herein, lead to partial pain relief at 2 hours in at least at least 63% of the treated human subjects.

In some embodiments, the methods of using a stable oral liquid pharmaceutical composition as disclosed herein, lead to an increase in the percentage of treated human subjects being pain free at 2 hours that is at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, or more, in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg). In some embodiments, the methods lead to an increase in the percentage of treated human subjects being partially relieved of pain at 2 hours that is at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, or more, in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg). In some embodiments, the methods lead to an increase in the percentage of treated human subjects being pain free at 2 hours that is at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, or more, in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg).

In some embodiments, the methods, comprising administering a composition as disclosed herein, lead to an increase in the percentage of treated human subjects being pain free at 2 hours that is at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, or more, in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg).

Some embodiments disclosed herein provide methods of treating pain in a human subject, the method comprising administering to the subject a stable oral liquid pharmaceutical composition, comprising a therapeutically effective amount of celecoxib, at least one solubilizer, at least one polar solvent, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, wherein the stable oral liquid pharmaceutical composition is essentially free of precipitation inhibitors, wherein the therapeutically effective amount of celecoxib is sufficient to render the subject pain free, or partially relieved of pain, lasting for at least 4 hours, at least 6 hours, at least 8 hours, at least 10 hours, at least 12 hours, at least 16 hours, at least 18 hours, at least 24 hours, at least 48 hours, or more, after administering the stable oral liquid pharmaceutical composition. In some embodiments, the stable oral liquid pharmaceutical composition comprises a therapeutically effective amount of celecoxib, at least one solubilize in amount from about 35 w/w to about 45 w/w, at least one polar solvent in amount from about 25% w/w to about 42% w/w, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, wherein the stable oral liquid pharmaceutical composition is essentially free of precipitation inhibitors. In some embodiments, the pain is associated with migraine. In some embodiments, the therapeutically effective amount of celecoxib is sufficient to render the subject pain free within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, the therapeutically effective amount of celecoxib is sufficient to lead to partial pain relief in the subject within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to pain free lasting for at least 24 hours after treatment in at least 25% of the treated human subjects. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to pain free lasting for at least 24 hours after treatment in at least 45% of the treated human subjects. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being pain free lasting for at least 24 hours after treatment that is at least 40% in comparison to the percentage of human subjects being treated with a placebo. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being pain free lasting for at least 24 hours after treatment that is at least 10% in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg). In some embodiments disclosed herein the methods for providing pain freedom in a human subject suffering from pain involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein the wherein said pain freedom is maintained for at least about 2 hours to about 24 hours. In some embodiments disclosed herein the methods for providing pain freedom in a human subject suffering from pain involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said pain freedom is maintained for at least about 2 hours to about 24 hours.

In some embodiments, the present application relates to a method for reducing most bothersome symptoms in a human subject suffering from migraine, said method comprising administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib and at least one pharmaceutically acceptable excipient, whereby the subject is provided with a reduction in the most bothersome symptoms. In some embodiments disclosed herein provide methods of treating pain in a human subject, the method comprising administering to the subject a stable oral liquid pharmaceutical composition, comprising a therapeutically effective amount of celecoxib, at least one solubilizer, at least one polar solvent, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, wherein the stable oral liquid pharmaceutical composition is essentially free of precipitation inhibitors, wherein the therapeutically effective amount of celecoxib is sufficient to render the subject free of most bothersome symptoms such as nausea, phonophobia and photophobia within 10 min, 20 min, 30 min, 60 min, within 2 hours, within 4 hours, within 6 hours, within 12 hours, of administering the stable oral liquid pharmaceutical composition. In some embodiments, the method for reducing the most bothersome symptoms in a human subject suffering from migraine involves administering to the subject a stable oral pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said most bothersome symptoms are reduced within about 2 hours of administration of said composition. In some embodiments, the method for reducing the most bothersome symptoms in a human subject suffering from migraine involves administering to the subject a stable oral liquid pharmaceutical composition comprising a therapeutically effective amount of celecoxib, wherein said most bothersome symptoms are reduced within about 2 hours of administration of said composition. In some embodiments, In some embodiments, the stable oral liquid pharmaceutical composition comprises a therapeutically effective amount of celecoxib, at least one solubilizer in amount from about 35% w/w to about 45% w/w, at least one polar solvent in amount from about 25% w/w to about 42% w/w, at least one medium chain glyceride, and at least one pharmaceutically acceptable excipient, wherein the stable oral liquid pharmaceutical composition is essentially free of precipitation inhibitors. In some embodiments, the pain is associated with migraine. In some embodiments, the therapeutically effective amount of celecoxib is sufficient to render the subject pain free within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, the therapeutically effective amount of celecoxib is sufficient to lead to partial pain relief in the subject within 2 hours of administering the stable oral liquid pharmaceutical composition. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to free of most bothersome symptoms within 2 hours of treatment in at least 25% of the treated human subjects. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to free of most bothersome symptoms within 2 hours of treatment in at least 45% of the treated human subjects. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being free of most bothersome symptoms within 2 hours of treatment that is at least 40% in comparison to the percentage of human subjects being treated with a placebo. In some embodiments, administering the stable oral liquid pharmaceutical composition leads to an increase in the percentage of treated human subjects being free of most bothersome symptoms within 2 hours of treatment that is at least 10% in comparison to the percentage of treated human subjects with a commercially available migraine pain treatment, such as VIOXX 25 (25 mg), VIOXX 50 (50 mg) and CAMBIA 50 (50 mg).

Some embodiments of the methods described herein further involve obtaining a report from the subject following administration. The report can be, for example, a report of a level of pain following administration. Such level of pain can be compared to a level of pain reported by the subject prior to administration, and in this regard, some embodiments of the methods further involve obtaining a report from the subject prior to administration. In addition to a report of level of pain following administration, other examples of reports that can be obtained from the subject following administration include a time point at which pain relief is rendered, a time point at which pain freedom is rendered, a time point at which freedom from most bothersome symptoms is rendered, a time period for which pain relief is maintained, a time period for which pain freedom is maintained, and a time period for which freedom from most bothersome symptoms is maintained.

In some embodiments, the oral liquid compositions of the present application can be dispensed in liquid form packaged in bottles or any other suitable containers for oral administration. The liquid composition can be ingested with or without further mixing with aqueous or suitable media before oral administration.

In some embodiments, the oral liquid compositions of the present application can be dispensed in container such as a sachet, ampoule, syringe or dropper device or tube or bottle, (for example, a tube or bottle which can be squeezed to deliver its contents), optionally as a fixed dosage, the contents of which may be directly orally ingested or mixed or dispersed into food or liquid.

In some embodiments, the compositions of present application can be formulated as capsule that is suitable for oral administration. The composition can be filled in hard or soft gelatin capsule or HPMC capsules or capsules made up of any other pharmaceutically acceptable materials.

In some embodiments, the composition of present application can be sprayed on inert substrate which can be a powder or a multiparticulate such as a granule, a pellet, a bead, a spherule, a beadlet, a microcapsule, a millisphere, a nanocapsule, a nanosphere or a microsphere.

A substrate constitutes a finely divided (milled, micronized, nanosized, precipitated) form of an inert additive molecular aggregates or a compound aggregate of multiple components or a physical mixture of aggregates of additives. Such substrates can be formed of various materials known in the art, such as, for example: sugars, such as lactose, sucrose or dextrose; polysaccharides, such as maltodextrin or dextrates; starches; cellulosics, such as microcrystalline cellulose or microcrystalline cellulose/sodium carboxymethyl cellulose; inorganics, such as dicalcium phosphate, hydroxyapatite, tricalcium phosphate, talc, or titanium dioxide; and polyols, such as mannitol, xylitol, sorbitol or cyclodextrin.

EXAMPLES

The following examples are offered to illustrate but not to limit the invention.

Although the invention has been illustrated by the following examples, it is not to be construed as being limited thereby; but rather, the invention encompasses the generic area as hereinbefore disclosed. Various modifications and embodiments can be made without departing from the spirit and scope thereof.

Examples 1-3: Stable Oral Compositions of Celecoxib used in the Studies

The compositions comprising celecoxib were prepared as given in Table 1.

TABLE 1 Stable oral liquid pharmaceutical compositions used in the studies. Example 1 Example 2 Example 3 Ingredients (% w/w) (% w/w) (% w/w) Celecoxib 5.00 5.00 4.76 Lauroyl 4.17 10.00 9.52 macrogolglycerides Glyceryl 5.00 5.00 4.76 Monocaprylate Glyceryl 12.50 12.50 11.90 Tricaprylate/Tricaprate Polyoxyl 35 castor oil 25.00 29.50 28.09 PEG-40 Hydrogenated 10.33 0.00 0.00 Castor Oil Sweeteners 8.65 8.65 1.47 Propyl gallate 0.02 0.02 0.00 Menthol 0.31 0.31 0.18 Flavors 1.46 1.46 0.32 Ethanol 20.00 20.00 0.00 Glycerine 5.21 5.21 0.00 Propylene glycol 0.00 0.00 33.87 Purified water q.s to 100 q.s to 100 q.s to 100

Manufacturing Procedure:

1. Celecoxib was added to solubilizers (lauroyl macrogolglycerides, polyoxyl 35 castor oil and PEG-40 Hydrogenated Castor Oil) and mixed properly to obtain uniform mixture.

2. Further to mixture of step 1 medium chain glycerides (caprylic/capric triglyceride and glyceryl caprylate) were added.

3. To the mixture of step 2, other ingredients such as flavors and sweeteners were added and mixed well.

4. To the composition of step 3, propylene glycol was added and mixed thoroughly with slight heating 30° C.±5° C. until a uniform dispersion is obtained and cool the solution to 25-30° C. under stirring.

5. To the composition of step 4, purified water was added and mixed well until a clear solution obtained.

6. The composition of step 5 was filled in amber colored glass bottle with 18 mm child resistant—tamper evident cap.

Example 4: Evaluation of Onset of Precipitation of the Stable Oral Composition

Compositions of Examples 1, 2 & 3 were evaluated for onset of precipitation time.

2 ml of compositions comprising 100 mg of celecoxib were dropped in 250 mL of FaSSGF, pH 2.0, at 37° C. under stirring and onset of precipitation was noted.

TABLE 2 Time for onset of precipitation. Time for onset of precipitation (minutes) Composition 30 60 120 180 240 Example 1 Precipitation Precipitation Precipitation Precipitation Precipitation not not not not not observed observed observed observed observed Example 2 Precipitation Precipitation Precipitation Precipitation Precipitation not not not not not observed observed observed observed observed Example 3 Precipitation Precipitation Precipitation Precipitation Precipitation not not not not not observed observed observed observed observed

Example 5: Evaluation of Dissolution Release Profile of the Stable Oral Compositions

Celecoxib dissolution study of 2 ml of the compositions of Examples 1, 2 & 3 comprising 100 mg of celecoxib was performed in a standard USP dissolution medium under the following conditions: USP apparatus II paddles; dissolution medium (900 ml 0.01N HCl containing 0.5% sodium lauryl sulfate) at a speed of 50 rpm and a temperature of 37° C.

TABLE 3 Dissolution of the stable oral composition in standard USP dissolution medium. Example 1 Example 2 Example 3 Sr. No Time (mins) % Released 1 10 >70 >70 >70 2 15 >80 >80 >80

Example 6: Evaluation of Physical Properties of Stable Oral Compositions

The composition of Example 3 was found to be stable after subjecting it to stability evaluation conditions of 25° C./60% RH and 40° C./75% RH. The composition was also evaluated for viscosity, density, pH, oil droplet size.

TABLE 4 Physical evaluation of the stable oral composition. Storage container Amber color glass bottle with cap 25° C./60% 40° C./75% RH RH Parameter Initial 1 Month 2 Month 3 Month 3 Month Assay 101.2 99.4 100 102.6 103.3 pH 5.93 5.92 5.85 5.58 5.77 Single 0.03 0.02 0.02 0.01 0.02 highest unknown impurity Total 0.05 0.02 0.02 0.01 0.02 impurity Density 1.01 1.01 1.01 1.011 1.017 (g/ml) Viscosity 129 108.9 104.6 101.6 127.7 (cps) D50 oil 18.4 18.1 18.7 18.4 18.1 droplet size D90 oil 27.5 26.6 27.6 27.6 26.7 droplet size

Example 7: Bioavailability of the Stable Oral Composition

A four-way, randomized, crossover study to compare the bioavailability of Example 3 (Celecoxib Oral Solution) at doses of 120 mg, 180 mg and 240 mg versus CELEBREX® (celecoxib) 400 mg capsules and to determine dose-proportionality of Example 3 formulations in healthy volunteers under fasting conditions.

In each study period, a single dose of celecoxib composition was administered orally, in the morning, following a 10-hour overnight fast. The administration is done as follows:

Treatment-1: Composition of Example 3 containing 120 mg of Celecoxib, administered orally to the volunteers followed by about 240 ml of water.

Treatment-2: Composition of Example 3 containing 180 mg of Celecoxib, administered orally to the volunteers followed by about 240 ml of water.

Treatment-3: Composition of Example 3 containing 240 mg of Celecoxib, administered orally to the volunteers followed by about 240 ml of water.

Treatment-4: An oral 400 mg dose (1×400 mg) CELEBREX® capsule was administered with about 240 mL of water.

Results:

Celecoxib plasma concentrations and other pharmacokinetic parameters were determined. Observed pharmacokinetic parameters are given in Table 5.

TABLE 5 Pharmacokinetic parameters after administration of the stable oral composition. Treatment-1 Treatment-2 Treatment-3 Treatment-4 (Test 120 mg) (Test 180 mg) (Test 240 mg) (Reference 400 mg) Parameters Mean ± SD Mean ± SD Mean ± SD Mean ± SD T_(lag) ^(a) 4.8 mins 4.8 mins 3.0 mins 10.2 mins (0.0-7.2) (0.0-7.2) (0.0-7.2) (4.8-19.8) T_(max) ^(a) (hrs) 0.67 (0.50-1.67) 0.67 (0.50-1.03) 0.95 (0.50-2.00) 2.50 (1.67-5.00) C_(max) 1061.909 ± 237.632 1544.886 ± 289.851  1932.543 ± 305.703 611.382 ± 222.223 (ng/mL) AUC₀_15 min  19.171 ± 10.697 26.616 ± 11.819  35.155 ± 17.795 0.300 ± 0.274 (ng · h/mL) AUC₀_30 min 149.120 ± 50.983 227.989 ± 68.623  283.211 ± 80.932  9.491± 5.773 (ng · h/mL) AUC_(0-1 hour)  604.826 ± 165.795 929.510 ± 193.524 1151.831 ± 214.121 103.166 (ng*h/mL)  61.783 AUC_(0-2 hours) 1322.703 ± 248.613 1976.926 ± 382.453  2621.176 ± 378.846 512.474 ± 292.137 (ng*h/mL) AUC_(0-t) 3059.684 ± 985.206 4633.125 ± 1478.184  6621.564 ± 1840.041 7288.003 ± 2505.792 (ng · h/mL) AUC_(0-∞)  3476.866 ± 1176.823 5234.806 ± 1423.726  6826.990 ± 1857.487 8074.908 ± 2159.266 (ng · h/mL) ^(a)Median (range)

Example 8: Study on Treatment of Migraine using the Stable Oral Composition

A three-way, double blind, randomized, crossover study was designed to determine efficacy of Example 3 (Celecoxib Oral Solution) at doses of 120 mg and 240 mg versus placebo in treating migraine. 60 subjects with history of 2-6 episodic migraine were recruited.

In each study period, a single dose of the stable oral composition was administered orally, in the morning, following a 10-hour overnight fast. The administration is done as follows:

-   -   Treatment-1: Composition of Example 3 containing 120 mg of         Celecoxib, administered orally to the volunteers followed by         about 240 ml of water.     -   Treatment-2: Composition of Example 3 containing 240 mg of         Celecoxib, administered orally to the volunteers followed by         about 240 ml of water.     -   Treatment-3: Placebo administered orally to the subjects,         followed by about 240 ml of water.

The subjects were monitored for pain at 2 hours and 24 hours and most bothersome symptom (MBS) at 2 hours following the administration.

Study medication was used once at the onset of moderate to severe migraine pain (defined as patient headache pain rating of 2 or 3 on a scale of 0 to 3), during each migraine attack, but no later than 1 hour after the onset of moderate migraine pain.

Patients were asked to rate the severity of their headache pain on a scale of 0 (no pain) to 3 (severe pain), which is the recommended method of obtaining patient headache pain ratings (Ref: Guidelines for controlled trials of drugs in migraine: Third edition. A guide for investigators” Tfelt-Hansen P, Pascual J, Ramadan N, et al. Cephalalgia, 2012; 32(1):6-38).

The ratings were obtained immediately prior to intake of study medication (time 0) and at 10, 15, 20, and 30 minutes and 1, 2, 1.5, 2, 24, and 48 hours postdose. Ratings were recorded by the patient in the eDiary for each migraine treated during the study. The severity rating scale was also used to assess the recurrence of headache pain following headache pain freedom during the 24 hours postdose. The recordings also include any recurrence of headache pain following headache pain freedom using headache pain severity rating scale during the 24 hours after study medication use; symptoms (nausea, photophobia, and phonophobia); rescue medication usage (date, time); functional disability; and patient-satisfaction (before using rescue medication).

The results of the above clinical study were shown in FIG. 4, FIG. 5, FIG. 6, FIG. 7 and Table 6 and 7.

TABLE 6 Primary Efficacy Analysis on Headache Pain Freedom: ITT Population, Observed Cases, Overall Treatment Period Treatment 3 Treatment 1 Treatment 2 Free of headache pain at 2 hours postdose Number of patients 52 50 49 Number of assessments 43 42 43 Response rate 18.6% 31.0% 25.6% Abbreviations: ITT = intention to treat. Note: Response rate (%) is calculated as the number of patients who responded at a given time point divided by the number patients with a nonmissing assessment at that time point. Note: P-value comes from a McNemar's test on independent pairs. ‘—’ indicates the test cannot be performed due to lack of paired data. An exact test is applied when there are fewer than 20 discordant pairs.

TABLE 7 Secondary Efficacy Analyses on the Most Bothersome Symptom: ITT Population, Last Observation Carried Forward Treatment 3 Treatment 1 Treatment 2 Placebo 120 mg 240 mg N = 53 N = 51 N = 51 Free of the most bothersome symptom at 2 hours postdose Number of evaluable patients 39 38 38 Response rate 28.2% 50.0% 39.5% Free of the most bothersome symptom (nausea) at 2 hours postdose Number of evaluable patients 12 5 10 Response rate 33.3% 60.0% 50.0% Free of the most bothersome symptom (photophobia) at 2 hours postdose Number of evaluable patients 20 22 19 Response rate 30.0% 50.0% 31.6% Free of the most bothersome symptom (photophobia) at 2 hours postdose Number of evaluable patients 7 11 9 Response rate 14.3% 45.5% 44.4% Abbreviations: ITT = intention to treat. Note: Response rate (%) is calculated as the number of patients who responded at a given time point divided by the number patients with a nonmissing assessment at that time point. Note: P-value comes from a McNemar's test on independent pairs. ‘—’ indicates the test cannot be performed due to lack of paired data. An exact test is applied when there are fewer than 20 discordant pairs.

In at least some of the previously described embodiments, one or more elements used in an embodiment can interchangeably be used in another embodiment unless such a replacement is not technically feasible. It will be appreciated by those skilled in the art that various other omissions, additions, and modifications may be made to the methods and structures described above without departing from the scope of the claimed subject matter. All such modifications and changes are intended to fall within the scope of the subject matter, as defined by the appended claims.

With respect to the use of substantially any plural and/or singular terms herein, those having skill in the art can translate from the plural to the singular and/or from the singular to the plural as is appropriate to the context and/or application. The various singular/plural permutations may be expressly set forth herein for sake of clarity.

It will be understood by those within the art that, in general, terms used herein, and especially in the appended claims (e.g., bodies of the appended claims) are generally intended as “open” terms (e.g., the term “including” should be interpreted as “including but not limited to,” the term “having” should be interpreted as “having at least,” the term “includes” should be interpreted as “includes but is not limited to,” etc.). It will be further understood by those within the art that if a specific number of an introduced claim recitation is intended, such an intent will be explicitly recited in the claim, and in the absence of such recitation, no such intent is present. For example, as an aid to understanding, the following appended claims may contain usage of the introductory phrases “at least one” and “one or more” to introduce claim recitations. However, the use of such phrases should not be construed to imply that the introduction of a claim recitation by the indefinite articles “a” or “an” limits any particular claim containing such introduced claim recitation to embodiments containing only one such recitation, even when the same claim includes the introductory phrases “one or more” or “at least one” and indefinite articles such as “a” or “an” (e.g., “a” and/or “an” should be interpreted to mean “at least one” or “one or more”); the same holds true for the use of definite articles used to introduce claim recitations. In addition, even if a specific number of an introduced claim recitation is explicitly recited, those skilled in the art will recognize that such recitation should be interpreted to mean at least the recited number (e.g., the bare recitation of “two recitations,” without other modifiers, means at least two recitations, or two or more recitations). Furthermore, in those instances where a convention analogous to “at least one of A, B, and C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, and C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). In those instances where a convention analogous to “at least one of A, B, or C, etc.” is used, in general, such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, or C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). It will be further understood by those within the art that virtually any disjunctive word and/or phrase presenting two or more alternative terms, whether in the description, claims, or drawings, should be understood to contemplate the possibilities of including one of the terms, either of the terms or both terms. For example, the phrase “A or B” will be understood to include the possibilities of “A” or “B” or “A and B.”

In addition, where features or aspects of the disclosure are described in terms of Markush groups, those skilled in the art will recognize that the disclosure is also thereby described in terms of any individual member or subgroup of members of the Markush group.

As will be understood by one of skill in the art, for any and all purposes, such as in terms of providing a written description, all ranges disclosed herein also encompass any and all possible sub-ranges and combinations of sub-ranges thereof. Any listed range can be easily recognized as sufficiently describing and enabling the same range being broken down into at least equal halves, thirds, quarters, fifths, tenths, etc. As a non-limiting example, each range discussed herein can be readily broken down into a lower third, middle third and upper third, etc. As will also be understood by one skilled in the art all language such as “up to,” “at least,” “greater than,” “less than,” and the like include the number recited and refer to ranges which can be subsequently broken down into sub-ranges as discussed above. Finally, as will be understood by one skilled in the art, a range includes each individual member. Thus, for example, a group having 1-3 articles refers to groups having 1, 2, or 3 articles. Similarly, a group having 1-5 articles refers to groups having 1, 2, 3, 4, or 5 articles, and so forth. 

What is claimed is:
 1. A method for providing pain freedom in a human subject suffering from pain, said method comprising administering to the subject a stable oral liquid pharmaceutical composition comprising: i. celecoxib in an amount from about 120 mg to about 240 mg; ii. at least one medium chain glyceride in an amount from about 5% to about 75% by weight, based on the total weight of the composition; and iii. at least one pharmaceutically acceptable excipient; wherein the at least one medium chain glyceride comprises glyceryl monocaprylate, glyceryl tricaprylate/tricaprate, or a combination thereof.
 2. The method of claim 1, wherein said pain freedom is maintained for at least about 2 hours to about 24 hours.
 3. The method of claim 1, wherein said composition is in the form of a solution, suspension, emulsion or liquid mixture.
 4. The method of claim 1, wherein said composition has a pH of from about 3 to about
 7. 5. The method of claim 1, where in the composition comprises a solubilizer and celecoxib in a weight ratio from about 4.0:1.0 to about 20:1.0.
 6. The method of claim 1, whereby the subject is provided with pain freedom at 2 hours following administration.
 7. The method of claim 1, wherein said composition further comprises at least one solubilizer in an amount from about 35% w/w to about 45% w/w, based on the total weight of the composition.
 8. The method of claim 1, further comprising a solubilizer and a polar solvent, wherein said solubilizer and polar solvent are present in a weight ratio of 0.60:1 to 1.8:1.
 9. The method of claim 1, wherein said composition further comprises at least one polar solvent in an amount from about 25% w/w to about 42% w/w, based on the total weight of the composition.
 10. A method for providing partial pain relief in a human subject suffering from pain, said method comprising administering to the subject a stable oral liquid pharmaceutical composition comprising: i. in an amount from about 120 mg to about 240 mg; ii. at least one medium chain glyceride in an amount from about 5% to about 75% by weight, based on the total weight of the composition; and iii. at least one pharmaceutically acceptable excipient; wherein the at least one medium chain glyceride comprises glyceryl monocaprylate, glyceryl tricaprylate/tricaprate, or a combination thereof.
 11. The method of claim 10, wherein said partial pain relief is at least ≥1 level lower pain intensity reported by the human subject suffering from pain, than the predose rating on a numeric rating scale for pain with a range of 0 (no pain) to 3 (severe).
 12. The method of claim 10, wherein said partial pain relief is maintained for at least about 4 hours.
 13. The method of claim 10, wherein said composition is in the form of a solution, suspension, emulsion or liquid mixture.
 14. The method of claim 10, wherein said composition has a pH of from about 3 to about
 7. 15. The method of claim 10, where in the composition comprises a solubilizer and celecoxib in a weight ratio from about 4.0:1.0 to about 20:1.0.
 16. The method of claim 10, wherein said composition further comprises at least one solubilizer in an amount from about 35% w/w to about 45% w/w, based on the total weight of the composition.
 17. The method of claim 10, further comprising a solubilizer and a polar solvent, wherein said solubilizer and polar solvent are present in a weight ratio of 0.60:1 to 1.8:1.
 18. The method of claim 10, wherein said composition further comprises at least one polar solvent in an amount from about 25% w/w to about 42% w/w, based on the total weight of the composition.
 19. A method for reducing nausea, photophobia and/or phonophobia in a human subject suffering from migraine, said method comprising administering to the subject a stable oral liquid pharmaceutical composition comprising: i. celecoxib in an amount from about 120 mg to about 240 mg; ii. at least one medium chain glyceride in an amount from about 5% to about 75% by weight, based on the total weight of the composition; and iii. at least one pharmaceutically acceptable excipient; wherein the at least one medium chain glyceride comprises glyceryl monocaprylate, glyceryl tricaprylate/tricaprate, or a combination thereof; whereby the subject is provided with a reduction in nausea, photophobia and/or phonophobia.
 20. The method of claim 19, wherein said composition is in the form of a solution, suspension, emulsion or liquid mixture.
 21. The method of claim 19, wherein said composition has a pH of from about 3 to about
 7. 22. The method of claim 19, where in the composition comprises a solubilizer and celecoxib in a weight ratio from about 4.0:1.0 to about 20:1.0.
 23. The method of claim 19, wherein said composition further comprises at least one solubilizer in an amount from about 35% w/w to about 45% w/w, based on the total weight of the composition.
 24. The method of claim 19, further comprising a solubilizer and a polar solvent, wherein said solubilizer and polar solvent are present in a weight ratio of 0.60:1 to 1.8:1.
 25. The method of claim 19, wherein said composition further comprises at least one polar solvent in an amount from about 25% w/w to about 42% w/w, based on the total weight of the composition. 